510(k) K023770 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM)
| Applicant | Kinetikos Medical, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Dec 12, 2002 |
| Received | Nov 12, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023770
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.