510(k) K081392 ยท HWC Screw, Fixation, Bone
BIORETEC ACTIVASCREW, ACTIVASCREW CANNULATED AND ACTIVASCREW CANNULATED WITH ACTIVAPIN
| Applicant | Bioretec, Ltd., Tampere, FI |
| Decision | Substantially Equivalent, Jun 18, 2008 |
| Received | May 19, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K081392
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.