510(k) K093086 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
ARTHROSTEER ABLATOR & COAGULATOR, MODELS: REF 1070 & 1080
| Applicant | Orthodynamix, LLC, Jacksonville FL, US |
| Decision | Substantially Equivalent, Feb 23, 2010 |
| Received | Oct 1, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093086
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.