ClearanceBrief
510(k) K140260 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

SKYHAWK LATERAL PLATE SYSTEM

ApplicantOrthofix, Inc., Lewisville TX, US
DecisionSubstantially Equivalent, Jul 2, 2014
ReceivedFeb 3, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K140260

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.