510(k) K121973 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
BIOPRO HEMI-EDGE TOE SYSTEM
| Applicant | Biopro, Inc., Prior Lake MN, US |
| Decision | Substantially Equivalent, Oct 30, 2012 |
| Received | Jul 5, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121973
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.