510(k) K101374 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation
AAXTER A3 POSTERIOR SPINAL SYSTEM
| Applicant | Aaxter Co., Ltd., Taipei, TW |
| Decision | Substantially Equivalent, Mar 16, 2011 |
| Received | May 17, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101374
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.