510(k) K171592 · MAI Fastener, Fixation, Biodegradable, Soft Tissue
CrossFT Knotless Biocomposite Suture Anchor with Disposable Driver
| Applicant | Conmed Corporation, Utica NY, US |
| Decision | Substantially Equivalent, Aug 29, 2017 |
| Received | May 31, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171592
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.