ClearanceBrief
510(k) K040168 ยท MQP Spinal Vertebral Body Replacement Device

MODIFICATION TO GEO STRUCTURE

ApplicantInterpore Cross Intl., Irvine CA, US
DecisionSubstantially Equivalent, Apr 8, 2004
ReceivedJan 26, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K040168

DateFirm and productCodeLinked 510(k)
Feb 4, 2005Interpore Cross International Inc
Spinal Implant, Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers)
Terminated
MQPNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.