510(k) K130196 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
SPEEDLOCK KNOTLESS FIXATION DEVICE, 3MM DRILL, 3MM+ DRILL, PATHFINDER OBTURATOR & SHARP TIPPED OBTURATOR, LOW PROFILE DR
| Applicant | Arthrocare Corp., Austin TX, US |
| Decision | Substantially Equivalent, Feb 27, 2013 |
| Received | Jan 28, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K130196
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.