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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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