ClearanceBrief
510(k) K061801 ยท JDR Staple, Fixation, Bone

2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS

ApplicantArthrotek, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Aug 7, 2006
ReceivedJun 26, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061801

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.