ClearanceBrief
510(k) K211320 ยท PLR Spinal Vertebral Body Replacement Device - Cervical

CAPRI Corpectomy Cage System

ApplicantK2m, Inc., Leesburg VA, US
DecisionSubstantially Equivalent, Feb 24, 2022
ReceivedApr 30, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K211320

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.