510(k) K181513 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
Arthrex PushLock Tenodesis Anchor
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Aug 30, 2018 |
| Received | Jun 8, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K181513
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.