510(k) K121890 ยท MAI Fastener, Fixation, Biodegradable, Soft Tissue
GENESYS PRESSFT SUTURE ANCHOR
| Applicant | Linvatec Corporation D/B/A Conmed Linvatec, Largo FL, US |
| Decision | Substantially Equivalent, Aug 22, 2012 |
| Received | Jun 28, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121890
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.