510(k) K003893 ยท HRX Arthroscope
VULCAN ABLATOR ELECTROSURGICAL PROBES, VULCAN LIGAMENT CHISEL ELECTROSURGICAL PROBES, MODEL 91000X,91002X,91300X
| Applicant | Oratec Interventions, Inc., Menlo Park CA, US |
| Decision | Substantially Equivalent, Mar 1, 2001 |
| Received | Dec 18, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003893
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.