510(k) K881378 ยท LXI Guide, Drill, Ligament
PFIZER HOSPITAL PRODUCTS GROUP ACL DRILL GUIDE
| Applicant | Pfizer, Inc., Groton CT, US |
| Decision | Substantially Equivalent, Jun 17, 1988 |
| Received | Apr 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881378
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.