ClearanceBrief
510(k) K950045 ยท JEY Plate, Bone

KLS-MARTIN MANDIBULAR FRACTURE/RECONSTRUCTION SYSTEM

ApplicantKarl Leibinger GmbH U. Co. KG, Washington DC, US
DecisionSubstantially Equivalent, Mar 23, 1995
ReceivedJan 5, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950045

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.