ClearanceBrief
510(k) K913688 ยท JEY Plate, Bone

BUD MAXILLOFACIAL IMPLANT SYSTEM

ApplicantBud Industries, Inc., Holland NY, US
DecisionSubstantially Equivalent, May 5, 1992
ReceivedAug 19, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913688

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.