ClearanceBrief
510(k) K180022 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

Athena Cervical Plate System

ApplicantMedyssey USA, Inc., Elk Grove Village IL, US
DecisionSubstantially Equivalent, Jul 20, 2018
ReceivedJan 3, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180022

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.