510(k) K132099 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
ARTHROCARE COBLATOR IQ DLR SPINEWAND, ARTHROCARE COBLATOR IQ DLG SPINEWAND
| Applicant | ArthroCare Corporation, Austin TX, US |
| Decision | Substantially Equivalent, Aug 22, 2013 |
| Received | Jul 8, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132099
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.