ClearanceBrief
510(k) K091426 ยท MQP Spinal Vertebral Body Replacement Device

CERVICORE CORPECTOMY CAGE

ApplicantVerticor, Ltd., Round Rock TX, US
DecisionSubstantially Equivalent, Dec 23, 2009
ReceivedMay 13, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K091426

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.