510(k) K071456 ยท MAI Fastener, Fixation, Biodegradable, Soft Tissue
ARTHREX PROSTOP PLUS ARTHROEREISIS SUBTALAR IMPLANT
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Jan 17, 2008 |
| Received | May 25, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071456
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.