ClearanceBrief
510(k) K093057 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

BIOMET VISION FOOTRING SYSTEM

ApplicantEbi, L.P., Parsippany NJ, US
DecisionSubstantially Equivalent, Dec 1, 2009
ReceivedSep 30, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K093057

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.