510(k) K090839 ยท HRS Plate, Fixation, Bone
MODIFICATION TO SYNTEC-TAICHUN NON-STERILE BONE PLATE AND SCREW IMPLANTS
| Applicant | Syntec Scientific Corp., Taipei City, TW |
| Decision | Substantially Equivalent, Apr 24, 2009 |
| Received | Mar 27, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K090839
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.