ClearanceBrief
510(k) K042571 ยท MQP Spinal Vertebral Body Replacement Device

STRYKER SPINE AVS TL PEEK SPACER

ApplicantStryker Spine, Allendale NJ, US
DecisionSubstantially Equivalent, Feb 11, 2005
ReceivedSep 21, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K042571

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.