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. |
| K240703 |
03/14/2024 |
Fine OsteotomyÖ |
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. |
|
|
