510(k) K061089 ยท KYI Prosthesis, Wrist, Carpal Trapezium
MODULAR THUMB IMPLANT, MODELS 17600, 17601, 17602, 17603, 17596, 17597, 17598, 17599
| Applicant | Biopro, Inc., Port Huron MI, US |
| Decision | Substantially Equivalent, Jun 20, 2006 |
| Received | Apr 18, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061089
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.