510(k) K240268 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
Accu-Joint Hemi Implant
| Applicant | Accufix Surgical, Inc., West Haven CT, US |
| Decision | Substantially Equivalent, Feb 29, 2024 |
| Received | Jan 31, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K240268
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.