510(k) K090815 ยท HRX Arthroscope
PERCUTANEOUS DISCECTOMY SYSTEM
| Applicant | Laurimed, LLC, Redwood City CA, US |
| Decision | Substantially Equivalent, May 21, 2009 |
| Received | Mar 25, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090815
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.