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

  • B278KTAGB505E0 ()
KTAGB505E

  • Knee arthroplasty wedge
TIBIAL AUGMENT, NONPOROUS, SIZE 4 X 15MM
ONKOS SURGICAL, INC.
KTAGB415E
In Commercial Distribution

  • B278KTAGB415E0 ()
KTAGB415E

  • Knee arthroplasty wedge
TIBIAL AUGMENT, NONPOROUS, SIZE 4 X 10MM
ONKOS SURGICAL, INC.
KTAGB410E
In Commercial Distribution

  • B278KTAGB410E0 ()
KTAGB410E

  • Knee arthroplasty wedge
TIBIAL AUGMENT, NONPOROUS, SIZE 4 X 5MM
ONKOS SURGICAL, INC.
KTAGB405E
In Commercial Distribution

  • B278KTAGB405E0 ()
KTAGB405E

  • Knee arthroplasty wedge
TIBIAL AUGMENT, NONPOROUS, SIZE 3 X 15MM
ONKOS SURGICAL, INC.
KTAGB315E
In Commercial Distribution

  • B278KTAGB315E0 ()
KTAGB315E

  • Knee arthroplasty wedge
TIBIAL AUGMENT, NONPOROUS, SIZE 3 X 10MM
ONKOS SURGICAL, INC.
KTAGB310E
In Commercial Distribution

  • B278KTAGB310E0 ()
KTAGB310E

  • Knee arthroplasty wedge
TIBIAL AUGMENT, NONPOROUS, SIZE 3 X 5MM
ONKOS SURGICAL, INC.
KTAGB305E
In Commercial Distribution

  • B278KTAGB305E0 ()
KTAGB305E

  • Knee arthroplasty wedge
TIBIAL AUGMENT, NONPOROUS, SIZE 2 X 15MM
ONKOS SURGICAL, INC.
KTAGB215E
In Commercial Distribution

  • B278KTAGB215E0 ()
KTAGB215E

  • Knee arthroplasty wedge
TIBIAL AUGMENT, NONPOROUS, SIZE 2 X 10MM
ONKOS SURGICAL, INC.
KTAGB210E
In Commercial Distribution

  • B278KTAGB210E0 ()
KTAGB210E

  • Knee arthroplasty wedge
TIBIAL AUGMENT, NONPOROUS, SIZE 2 X 5MM
ONKOS SURGICAL, INC.
KTAGB205E
In Commercial Distribution

  • B278KTAGB205E0 ()
KTAGB205E

  • Knee arthroplasty wedge
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