510(k) K012305 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
MODIFICATION TO: TRINICA ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Sulzer Spine-Tech, Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 22, 2001 |
| Received | Jul 23, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012305
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.