510(k) K003984 ยท MAI Fastener, Fixation, Biodegradable, Soft Tissue
SUPER REVO SUTURE ANCHOR
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Mar 19, 2001 |
| Received | Dec 26, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003984
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.