ClearanceBrief
510(k) K033355 ยท HWC Screw, Fixation, Bone

LACTOSCREW SCREW ANCHOR

ApplicantBiomet Orthopedics, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Jun 30, 2004
ReceivedOct 20, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033355

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.