510(k) K080879 ยท HTY Pin, Fixation, Smooth
ACTIVATM PRODUCT GROUP INCLUDING BIOABSORBABLE DEVICES ACTIVAPIN FUSION, ACTIVANAILTM CONICALTM
| Applicant | Bioretec, Ltd., Tampere, FI |
| Decision | Substantially Equivalent, Jun 24, 2008 |
| Received | Mar 31, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080879
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.