510(k) K063052 ยท JEY Plate, Bone
LORENZ TITANIUM FRACTURE / RECONSTRUCTION DEVICES AND PRE-BENT PLATES
| Applicant | Walter Lorenz Surgical, Inc., Jacksonville FL, US |
| Decision | Substantially Equivalent, Jan 12, 2007 |
| Received | Oct 4, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063052
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.