510(k) K950011 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
COHORT(TM) ANTERIOR PLATE SYSTEM (APS)
| Applicant | Cohort Medical Products Group, Inc., Hayward CA, US |
| Decision | Substantially Equivalent for Some Indications, Nov 6, 1995 |
| Received | Jan 3, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950011
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.