ClearanceBrief
Recall Z-0530-05 ยท MQP Spinal Vertebral Body Replacement Device

Interpore Cross International Inc

Spinal Implant, Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers)

DateFeb 4, 2005 (initiated Jan 14, 2005)
StatusTerminated
ReasonMislabeled.
Root causeOther
ActionFirm sent recall letters on 1/18/2005 requesting return of product. A response form was enclosed.
Quantity63
DistributionTN, MT, MI, CA, IN, PA, NJ, TX, KY, LA, CO.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K040168MODIFICATION TO GEO STRUCTURE
Interpore Cross Intl., Apr 8, 2004