ClearanceBrief
510(k) K961976 ยท JEY Plate, Bone

THE BIOPLATE FIXATION SYSTEM

ApplicantBiomedics, Washington DC, US
DecisionSubstantially Equivalent, Aug 16, 1996
ReceivedMay 20, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961976

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.