ClearanceBrief
510(k) K920213 ยท JDR Staple, Fixation, Bone

MITEK ANCHOR, MITEK ANCHOR II

ApplicantMitek Surgical Products, Inc., Norwood MA, US
DecisionSubstantially Equivalent, May 1, 1992
ReceivedJan 16, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920213

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.