ClearanceBrief
510(k) K061389 ยท JDR Staple, Fixation, Bone

ALLTHREAD LACTOSORB SUTURE ANCHOR

ApplicantArthrotek, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Jul 19, 2006
ReceivedMay 18, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061389

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.