510(k) K041713 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
SUPER REVO HERCULINE SUTURE ANCHOR
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Jul 22, 2004 |
| Received | Jun 23, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K041713
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.