ClearanceBrief
510(k) K061836 ยท MQP Spinal Vertebral Body Replacement Device

AVS ASL PEEK SPACER SYSTEM

ApplicantStryker Spine, Allendale NJ, US
DecisionSubstantially Equivalent, Aug 3, 2006
ReceivedJun 29, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K061836

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.