510(k) K093717 ยท HRX Arthroscope
C-MOR VISUALIZATION DEVICE
| Applicant | Axis Surgical Technologies, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Mar 2, 2010 |
| Received | Dec 2, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093717
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.