ClearanceBrief
510(k) K981798 ยท JDR Staple, Fixation, Bone

LACTOSORB POP RIVET

ApplicantBiomet, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Jul 13, 1998
ReceivedMay 21, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K981798

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.