ClearanceBrief
510(k) K083469 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal

METASURG CANNULATED TIATANIUM HEMI IMPLANT, MODEL HM-1000

ApplicantMetasurg, Houston TX, US
DecisionSubstantially Equivalent, Feb 13, 2009
ReceivedNov 24, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K083469

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.