ClearanceBrief
510(k) K062759 ยท MQP Spinal Vertebral Body Replacement Device

PARAMOUNT VBR SYSTEM

ApplicantInnovative Spinal Technologies, Inc., Mansfield MA, US
DecisionSubstantially Equivalent, Jan 12, 2007
ReceivedSep 15, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062759

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.