510(k) K030319 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
ORTHOSPHERE CERAMIC SPHERICAL IMPLANT
| Applicant | Wrightmedicaltechnologyinc, Arlington TN, US |
| Decision | Substantially Equivalent, Nov 26, 2003 |
| Received | Jan 30, 2003 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K030319
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.