510(k) K122662 ยท HRX Arthroscope
VERTIFLEX DIRECT DECOMPRESSION SYSTEM
| Applicant | Vertiflex, Inc., San Clamente CA, US |
| Decision | Substantially Equivalent, Nov 13, 2012 |
| Received | Aug 31, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122662
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.