ClearanceBrief
510(k) K113006 ยท HWC Screw, Fixation, Bone

I-FUSE HAMMER TOE SYSTEMS

ApplicantOrthopro, LLC, Round Rock TX, US
DecisionSubstantially Equivalent, May 25, 2012
ReceivedOct 7, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113006

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.