ClearanceBrief
510(k) K100012 ยท MAI Fastener, Fixation, Biodegradable, Soft Tissue

GRYPHON T BR DS ANCHOR W/ORTHOCORD, GRYPHON T BR ANCHOR W /ORTHOCORD, GRYPHON P BR DS ANCHOR W/ORTHOCORD, GRYPHON P BR A

ApplicantDepuy Mitek, A Johnson & Johnson Company, Raynham MA, US
DecisionSubstantially Equivalent, Apr 30, 2010
ReceivedJan 4, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K100012

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.