ClearanceBrief
510(k) K021341 ยท JEY Plate, Bone

NORMED BONE TRANSPORT DISTRACTION DEVICE

ApplicantOsteomedics, Inc., Paramus NJ, US
DecisionSubstantially Equivalent, Aug 1, 2002
ReceivedApr 29, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K021341

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.