ClearanceBrief
510(k) K040500 ยท HTY Pin, Fixation, Smooth

ARTHROTEK LACTONAIL

ApplicantArthrotek, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, May 25, 2004
ReceivedFeb 26, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K040500

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.