ClearanceBrief
510(k) K230301 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

Athena III Cervical Plate System

ApplicantMedyssey USA, Inc., Temecula CA, US
DecisionSubstantially Equivalent, Mar 7, 2023
ReceivedFeb 3, 2023
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K230301

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.