510(k) K062908 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
ORTHROPRO HEMI TOE
| Applicant | Orthopro, LLC, Round Rock TX, US |
| Decision | Substantially Equivalent, Nov 13, 2006 |
| Received | Sep 27, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062908
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.