ClearanceBrief
510(k) K060442 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

PYRENEES CERVICAL PLATE SYSTEM

ApplicantK2m, LLC, Leesburg VA, US
DecisionSubstantially Equivalent, May 15, 2006
ReceivedFeb 21, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060442

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.