510(k) K203634 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
BioPoly Great Toe Hemiarthroplasty Implant
| Applicant | BioPoly, LLC, Fort Wayne IN, US |
| Decision | Substantially Equivalent, Feb 2, 2021 |
| Received | Dec 11, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203634
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.