510(k) K982006 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
MICOMED - HALM ZIELKE INSTRUMENTATION
| Applicant | Micomed GmbH, Fullerton CA, US |
| Decision | Substantially Equivalent, Jan 20, 1999 |
| Received | Jun 8, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982006
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.