510(k) K011556 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
MACS HMA ANTERIOR SPINAL STABILIZATION SYSTEM
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Nov 16, 2001 |
| Received | May 21, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011556
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.