ClearanceBrief
510(k) K112861 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

SINTEA PLUSTEK ANTERIOR CERVICAL PLATE SYSTEM

ApplicantSintea Plustek, LLC, Miami Beach FL, US
DecisionSubstantially Equivalent, Feb 24, 2012
ReceivedSep 30, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K112861

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.