510(k) K090303 ยท HRX Arthroscope
XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004
| Applicant | Corespine Technologies, LLC, Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 30, 2009 |
| Received | Feb 6, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090303
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.