510(k) K014164 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
GREAT TOE IMPLANT SYSTEM
| Applicant | Harmos Orthopaedics, Inc., Cantonville MD, US |
| Decision | Substantially Equivalent, Mar 12, 2002 |
| Received | Dec 19, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014164
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.