ClearanceBrief
510(k) K231460 · KWQ Appliance, Fixation, Spinal Intervertebral Body

FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate System, BALTEUM™ & BALTEUM-ONE™ Lumbar Plate System, and Osprey™ Anterior Cervical Plate System

ApplicantK&J Consulting Corp., Lansdale PA, US
DecisionSubstantially Equivalent, Jul 16, 2023
ReceivedMay 19, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231460

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.