510(k) K031859 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
CAP GREAT TOE RESURFACING HEMI-ARTHROPLASTY IMPLANT
| Applicant | Arthrosurface, Inc., Stoughton MA, US |
| Decision | Substantially Equivalent, Feb 18, 2004 |
| Received | Jun 16, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031859
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.