ClearanceBrief
510(k) K992683 ยท JEY Plate, Bone

MODUS 2.5 MANDIBULAR TRAUMA SET

ApplicantMedartis AG, Waltham MA, US
DecisionSubstantially Equivalent, Nov 24, 1999
ReceivedAug 10, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992683

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.