510(k) K052596 ยท KYI Prosthesis, Wrist, Carpal Trapezium
MODULAR THUMB IMPLANT, MODELS 17065,17066,17243,17067,17199,17238,17005,17239,17006,17240,17007,17241,17500,17501,17507
| Applicant | Biopro, Inc., Port Huron MI, US |
| Decision | Substantially Equivalent, Nov 15, 2005 |
| Received | Sep 21, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052596
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.