ClearanceBrief
510(k) K040475 ยท HWC Screw, Fixation, Bone

MICROMAX SUTURE ANCHOR

ApplicantBiomet, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, May 21, 2004
ReceivedFeb 24, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K040475

DateFirm and productCodeLinked 510(k)
Jan 13, 2010Biomet, Inc.
Biomet 2.9 Micromax L-15 suture anchor, flexible long shaft, #2 blue/white maxbraid, PLLA/PGA L-15, sterile, Biomet Sports Medicine, Warsaw, IN; REF 905456. Intended for use in soft tissue reattachme
Terminated
HWCNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.