510(k) K133606 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
N8TIVE ACL ANATOMIC RECONSTRUCTION SYSTEM, N8TIVE ACL FEMORAL IMPLANT, N8TIVE ACL TIBIAL IMPLANT, VARIOUS CLASS I ANCILL
| Applicant | ArthroCare Corporation, Austin TX, US |
| Decision | Substantially Equivalent, Apr 1, 2014 |
| Received | Nov 25, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133606
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.