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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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LEGION FUL ANGLED WEDGE RESECTION GUIDE
Smith & Nephew, Inc.
71434344
Not in Commercial Distribution

  • 03596010549945 ()
71434344

  • Knee arthroplasty wedge
LEGION HEMI ANGLED WEDGE RESECTION GUIDE
Smith & Nephew, Inc.
71434343
Not in Commercial Distribution

  • 03596010549938 ()
71434343

  • Knee arthroplasty wedge
TIBIAL AUGMENT 5 / 4+ X 15° NONPOROUS 5 / 4+ X 15°
ONKOS SURGICAL, INC.
KTAGW515E
In Commercial Distribution

  • B278KTAGW515E0 ()
KTAGW515E

  • Knee arthroplasty wedge
TIBIAL AUGMENT 4 / 3+ X 15° NONPOROUS 4 / 3+ X 15°
ONKOS SURGICAL, INC.
KTAGW415E
In Commercial Distribution

  • B278KTAGW415E0 ()
KTAGW415E

  • Knee arthroplasty wedge
TIBIAL AUGMENT 3 / 2+ X 15° NONPOROUS 3 / 2+ X 15°
ONKOS SURGICAL, INC.
KTAGW315E
In Commercial Distribution

  • B278KTAGW315E0 ()
KTAGW315E

  • Knee arthroplasty wedge
TIBIAL AUGMENT 2 / 1+ X 15° NONPOROUS 2 / 1+ X 15°
ONKOS SURGICAL, INC.
KTAGW215E
In Commercial Distribution

  • B278KTAGW215E0 ()
KTAGW215E

  • Knee arthroplasty wedge
TIBIAL AUGMENT 1 X 15° NONPOROUS 1 X 15°
ONKOS SURGICAL, INC.
KTAGW115E
In Commercial Distribution

  • B278KTAGW115E0 ()
KTAGW115E

  • Knee arthroplasty wedge
TIBIAL AUGMENT, NONPOROUS, SIZE 5 X 15MM
ONKOS SURGICAL, INC.
KTAGB515E
In Commercial Distribution

  • B278KTAGB515E0 ()
KTAGB515E

  • Knee arthroplasty wedge
TIBIAL AUGMENT, NONPOROUS, SIZE 5 X 10MM
ONKOS SURGICAL, INC.
KTAGB510E
In Commercial Distribution

  • B278KTAGB510E0 ()
KTAGB510E

  • Knee arthroplasty wedge
TIBIAL AUGMENT, NONPOROUS, SIZE 5 X 5MM
ONKOS SURGICAL, INC.
KTAGB505E
In Commercial Distribution

  • B278KTAGB505E0 ()
KTAGB505E

  • Knee arthroplasty wedge
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