ClearanceBrief
510(k) K021967 ยท MQP Spinal Vertebral Body Replacement Device

HEDROCEL VERTEBRAL BODY REPLACEMENT, MODELS 06-112-00XX2 AND 06-132-10XX2

ApplicantImplex Corp., Allendale NJ, US
DecisionSubstantially Equivalent, Jul 17, 2002
ReceivedJun 17, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K021967

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.