510(k) K964975 ยท HRX Arthroscope
COHORT DISCECTOMY SYSTEMS (CDS)
| Applicant | Cohort Medical Products Group, Inc., Hayward CA, US |
| Decision | Substantially Equivalent, Feb 24, 1997 |
| Received | Dec 12, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964975
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.