ClearanceBrief
510(k) K053292 ยท MQP Spinal Vertebral Body Replacement Device

DAVANTIS/ANTELYS VERTEBRAL BODY REPLACEMENTS

ApplicantScient'X USA, Inc., Round Rock TX, US
DecisionSubstantially Equivalent, Jan 19, 2006
ReceivedNov 25, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K053292

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.