FDA 510(k) Applications Submitted by Bodycad Laboratories, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K191150 05/01/2019 Bodycad Unicompartmental Knee System Bodycad Laboratories, Inc.
K191996 07/26/2019 BC Reflex Uni Knee System Bodycad Laboratories, Inc.
K193614 12/26/2019 FINE Osteotomy around the knee Bodycad Laboratories, Inc.
K163700 12/29/2016 Bodycad Unicompartmental Knee System Bodycad Laboratories, Inc.
K231314 05/05/2023 Fine OsteotomyÖ BodyCad Laboratories, Inc.
K211646 05/28/2021 FINE Osteotomy Bodycad Laboratories, Inc.
K211895 06/21/2021 BC Reflex Uni Knee System Bodycad Laboratories, Inc.
K212307 07/23/2021 BC Reflex Uni Knee System Bodycad Laboratories, Inc.
K203697 12/18/2020 BC Reflex Uni Knee System Bodycad Laboratories, Inc.


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