ClearanceBrief
510(k) K062151 ยท MQP Spinal Vertebral Body Replacement Device

BOX PEEK VBR SYSTEM

ApplicantInnovasis, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Dec 22, 2006
ReceivedJul 27, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062151

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.