ClearanceBrief
510(k) K150771 ยท PBJ Cranial Distraction System

RxG Distraction System

ApplicantKLS Martin L.P., Jacksonville FL, US
DecisionSubstantially Equivalent, Aug 27, 2015
ReceivedMar 24, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K150771

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.