ClearanceBrief
510(k) K042930 ยท MQP Spinal Vertebral Body Replacement Device

SPACEVISION CAGE SYSTEM

ApplicantSpine Vision, Inc., Atlanta GA, US
DecisionSubstantially Equivalent, Dec 28, 2004
ReceivedOct 22, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K042930

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.