510(k) K071176 ยท MAI Fastener, Fixation, Biodegradable, Soft Tissue
MODIFICATION TO: ARTHREX INTERFERENCE SCREW
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Aug 3, 2007 |
| Received | Apr 27, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071176
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.