# K191150: Bodycad Unicompartmental Knee System

- Pathway: 510(k) (Traditional)
- Applicant: Bodycad Laboratories, Inc.
- Decided: Oct 8, 2019 after 160 days
- Product code: HSX (Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer)
- Device class: 2
- Regulation: 21 CFR 888.3520
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 12 generations back to K911802 (1992). 67 ancestors in all.
4 later devices descend from it; 3 cite it directly.
0 of 72 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K163700: Bodycad Unicompartmental Knee System, Bodycad Laboratories, Inc. (2017) Summary page 4.
- K181302: Bodycad Unicompartmental Knee System, Bodycad Laboratories, Inc. (2019) Summary page 4.

## Most influential descendants
- K191996: BC Reflex Uni Knee System (2019), 3 descendants of its own
- K203697: BC Reflex Uni Knee System (2021), 2 descendants of its own
- K212307: BC Reflex Uni Knee System (2021), 0 descendants of its own
- K211895: BC Reflex Uni Knee System (2021), 0 descendants of its own

## Indications for use
The patient-specific Bodycad Unicompartmental Knee System (Bodycad UKS) is indicated for unicompartmental knee arthroplasty (UKA) in patients with advanced knee osteoarthritis (OA) of the medial compartment with evidence of adequate healthy bone to support the implanted components. Candidates for unicompartmental knee replacement include those with: » joint impairment due to osteoarthritis or traumatic arthritis of the knee, » varus deformity of the knee, and » as an alternative to tibial osteotomy in patients with unicompartmental OA. The patient-specific Bodycad UKS components fit within an envelope of dimensions that are specific to each patient. The Bodycad UKS femoral component and tibial baseplate are intended for cemented fixation. A Bodycad screw must be used for fixation of the femoral component.

Source page: https://510kreport.com/device/K191150
Methodology: https://510kreport.com/methodology