510(k) K872502 ยท KWM Prosthesis, Wrist, Semi-Constrained
M.W.P. WRIST PROSTHESIS
| Applicant | Protek, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Jul 23, 1987 |
| Received | Jun 24, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872502
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.