ClearanceBrief
510(k) K101353 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

GOLDEN GATE ANTERIOR PLATE SYSTEM

ApplicantUlrich GmbH & Co. KG, St. Louis MO, US
DecisionSubstantially Equivalent, Feb 4, 2011
ReceivedMay 14, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K101353

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.