ClearanceBrief
510(k) K020522 ยท MQP Spinal Vertebral Body Replacement Device

MODIFICATION TO SURGICAL TITANIUM MESH SYSTEM

ApplicantDepuyacromed, Raynham MA, US
DecisionSubstantially Equivalent, Mar 21, 2002
ReceivedFeb 19, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K020522

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.