ClearanceBrief
510(k) K063370 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal

CAP 7.0MM MTP RESURFACING HEMI-ARTHROPLASTY

ApplicantArthrosurface, Inc., Franklin MA, US
DecisionSubstantially Equivalent, Jan 12, 2007
ReceivedNov 8, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K063370

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.