ClearanceBrief
510(k) K780187 ยท JDO Device, Fixation, Proximal Femoral, Implant

NAIL, MASSIE II

ApplicantHowmedica Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 15, 1978
ReceivedFeb 6, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780187

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.