Guide for localizing a nonpalpable breast lesion

Claim 2

A wire guide for localizing a nonpalpable lesion in a breast comprising: a straight portion; and a distal portion preformed into a resilient configuration of substantially more than a 180 degree turn, said distal portion including a superelastic material such that said resilient configuration of said distal portion can be repeatably and smoothly inserted into and smoothly withdrawn from the region of the lesion characterized in that said resilient configuration of said distal portion assumes an unwound configuration when positioned in a passageway of a tubular introducer needle, said distal position assuming a resilient helical coil configuration as said distal portion of said wire guide is extended from a passageway of a needle, said resilient helical coil configuration including a longitudinal passageway extending laterally from said straight portion.

Claim 3

A wire guide for localizing a nonpalpable lesion in a breast comprising: a straight portion; and a distal portion including a superelastic metallic alloy and having an unwound configuration when positioned in a passageway of a cannula and a preformed, resilient helical coil configuration extending laterally from said straight portion when positioned out of a passageway of a cannula.

Claim 4

A wire guide for localizing a nonpalpable lesion in a breast comprising: a straight portion; and a distal portion including a superelastic metallic alloy and having an unwound configuration when positioned in a passageway of a cannula and a preformed, resilient helical coil configuration extending laterally from said straight portion when positioned out of a passageway of a cannula.

Claim 5

The wire guide of claim 2 wherein said resilient helical coil configuration includes at least more than a 180 degree turn.

Claim 6

The wire guide of claim 2 wherein said resilient helical coil configuration of said distal portion includes an acuate distal end.

Claim 7

The wire guide of claim 2 further comprising a cannula including a passageway extending longitudinally therethrough.

Claim 8

The wire guide of claim 2 wherein said superelastic metallic alloy includes nickel and titanium.

Claim 9

The wire guide of claim 2 wherein said superelastic metallic alloy has a predetermined transformation temperature and wherein said superelastic metallic alloy is normally operated above said predetermined transformation temperature.

Claim 10

A medical device for localizing a nonpalpable lesion in a breast comprising: a tubular needle having a passageway extending longitudinally therethrough and a distal end tapered for insertion into said breast to the site of said lesion; and a wire guide for insertion into said passageway of said needle and having a straight portion and a distal portion, said distal portion including a superelastic metallic alloy, a preformed, resilient helical coil configuration extending laterally from said straight portion when positioned out of said passageway of said tubular needle, and an unwound configuration when positioned in said passageway of said tubular needle.

Claim 11

A medical device for localizing a nonpalpable lesion in a breast comprising: a tubular needle having a passageway extending longitudinally therethrough and a distal end tapered for insertion into said breast to the site of said lesion; and a wire guide for insertion into said passageway of said needle and having a straight portion and a distal portion, said distal portion including a superelastic metallic alloy, a preformed, resilient helical coil configuration extending laterally from said straight portion when positioned out of said passageway of said tubular needle, and an unwound configuration when positioned in said passageway of said tubular needle.

Claim 12

The device of claim 8 wherein said resilient helical coil configuration includes at least more than a 180 degree turn.

Claim 13

The device of claim 8 wherein said distal portion includes an acuate distal end.

Claim 14

The device of claim 8 wherein said resilient helical coil configuration of said distal portion includes at least one turn and an acuate distal end, said at least one turn following a path scribed by said acuate distal end as said distal portion is extended from said passageway of said needle.

Claim 15

The device of claim 8 wherein said superelastic metallic alloy includes nickel and titanium.

Claim 16

The device of claim 8 wherein said superelastic metallic alloy has a predetermined transformation temperature.

Claim 17

The device of claim 8 wherein said needle comprises a first cannula including said passageway and a predetermined interior surface about said passageway.

Claim 18

The device of claim 14 wherein said predetermined interior surface is a plug-drawn surface.

Claim 19

The device of claim 8 wherein said tubular needle has a plurality of indentations in an outer surface thereof about said tapered distal end.

Claim 20

The device of claim 16 wherein said indentations are at least partially semispherical.

Claim 21

A medical device for localizing a nonpalpable lesion in a breast comprising: a tubular needle comprising a first cannula having a passageway extending longitudinally therethrough, a predetermined interior surface about said passageway, and a distal end tapered for insertion into said breast to the site of said lesion; a wire guide for insertion into said passageway of said tubular needle and having a straight portion and a distal portion, said distal portion including a superelastic metallic alloy, a preformed, resilient helical coil configuration when positioned out of said passageway of said tubular needle, and an unwound configuration when positioned in said passageway of said tubular needle; and a second cannula having a distal end and a passageway extending longitudinally therethrough, said distal portion of said wire guide for insertion into said passageways of said first and second cannulas assuming said unwound configuration when positioned in said passageway of said second cannula, said first cannula including a proximal end, said distal end of said second cannula abutting against said proximal end of said first cannula when transferring said distal portion of said wire guide in said unwound configuration from said passageway of said second cannula to said passageway of said first cannula.

Claim 22

A medical device for localizing a nonpalpable lesion in a breast comprising: a tubular needle comprising a first cannula having a passageway extending longitudinally therethrough, a predetermined interior surface about said passageway, and a distal end tapered for insertion into said breast to the site of said lesion; a wire guide for insertion into said passageway of said tubular needle and having a straight portion and a distal portion, said distal portion including a superelastic metallic alloy, a preformed, resilient helical coil configuration when positioned out of said passageway of said tubular needle, and an unwound configuration when positioned in said passageway of said tubular needle; and a second cannula having a distal end and a passageway extending longitudinally therethrough, said distal portion of said wire guide for insertion into said passageways of said first and second cannulas assuming said unwound configuration when positioned in said passageway of said second cannula, said first cannula including a proximal end, said distal end of said second cannula abutting against said proximal end of said first cannula when transferring said distal portion of said wire guide in said unwound configuration from said passageway of said second cannula to said passageway of said first cannula.

Claim 23

The device of claim 18 further comprising a cap having a passageway extending longitudinally therein sized for receiving said first and second cannulas and aligning said passageways thereof.

Claim 24

A medical device for localizing a nonpalpable lesion in a breast comprising: a tubular introducer needle including a first cannula having a first distal end tapered for insertion into said breast to the site of said lesion, a first proximal end, a first passageway extending longitudinally between said first ends, a plug-drawn interior surface about said first passageways, and an outer surface having a plurality of semispherical indentations therein about said first distal end; a second cannula including a second distal end, a second proximal end, a second passageway extending longitudinally between said second ends and a second plug-drawn interior surface about said second passageway; a connector having a passageway extending longitudinally therein and sized for receiving said first and second cannulas and aligning said passageways thereof; and a wire guide for insertion in said first and second passageways of said first and second cannulas and having a straight portion and a distal portion, said distal portion including a superelastic, nickel and titanium metallic alloy and a preformed, resilient helical coil configuration including at least more than a 180 degree turn, an acuate distal end, and a passageway extending longitudinally through said preformed, resilient helical coil configuration and laterally from said straight portion, said alloy having a predetermined transformation temperature, said distal end portion assuming an unwound configuration when positioned in said first passageway of at least one of said first and second cannulas, said at least more than a 180 degree turn following a path scribed by said acuate distal end as said distal portion is extended from said first passageway at said tapered first distal end of said first cannula, said second distal end of said second cannula abutting against said first proximal end of said first cannula when transferring said distal portion of said wire guide in said unwound configuration from said second passageway of said second cannula to said first passageway of said first cannula.

Claim 25

A medical device for localizing a nonpalpable lesion in a breast comprising: a tubular introducer needle including a first cannula having a first distal end tapered for insertion into said breast to the site of said lesion, a first proximal end, a first passageway extending longitudinally between said first ends, a plug-drawn interior surface about said first passageways, and an outer surface having a plurality of semispherical indentations therein about said first distal end; a second cannula including a second distal end, a second proximal end, a second passageway extending longitudinally between said second ends and a second plug-drawn interior surface about said second passageway; a connector having a passageway extending longitudinally therein and sized for receiving said first and second cannulas and aligning said passageways thereof; and a wire guide for insertion in said first and second passageways of said first and second cannulas and having a straight portion and a distal portion, said distal portion including a superelastic, nickel and titanium metallic alloy and a preformed, resilient helical coil configuration including at least more than a 180 degree turn, an acuate distal end, and a passageway extending longitudinally through said preformed, resilient helical coil configuration and laterally from said straight portion, said alloy having a predetermined transformation temperature, said distal end portion assuming an unwound configuration when positioned in said first passageway of at least one of said first and second cannulas, said at least more than a 180 degree turn following a path scribed by said acuate distal end as said distal portion is extended from said first passageway at said tapered first distal end of said first cannula, said second distal end of said second cannula abutting against said first proximal end of said first cannula when transferring said distal portion of said wire guide in said unwound configuration from said second passageway of said second cannula to said first passageway of said first cannula.