ClearanceBrief
510(k) K080367 ยท FST Light, Surgical, Fiberoptic

ZIMMER MIS LIGHT

ApplicantZimmer Spine, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Feb 22, 2008
ReceivedFeb 12, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K080367

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.