510(k) K090278 ยท HRX Arthroscope
ENSPIRE DEBRIDER SYSTEM
| Applicant | Spine View, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Apr 15, 2009 |
| Received | Feb 4, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090278
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.