ClearanceBrief
510(k) K003155 ยท MQP Spinal Vertebral Body Replacement Device

VERTEBRAL BODY REPLACEMENT

ApplicantOsteotech, Inc., Eatontown NJ, US
DecisionSubstantially Equivalent, Jan 4, 2001
ReceivedOct 10, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K003155

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.