ClearanceBrief
510(k) K061657 ยท JDR Staple, Fixation, Bone

HITCH LACTOSORB SUTURE ANCHOR

ApplicantArthrotek, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Jul 25, 2006
ReceivedJun 13, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061657

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.