InjuryMBP
PRO OSTEON IMPLANT 500 CORRALINE HYDROXYAPATITE BONE VOID FI
Received Apr 29, 1997
Report 2029012-1997-00091 · MDR key 88830
Device
Generic name
Endosseous Implant
Manufacturer
Interpore Intl.Model number
NACatalog number
UNK
Lot number
UNK
Patient
40 YR
Narrative
Description of Event or Problem
A REPORT WAS RECEIVED INVOLVING DEVICE USED TO REPAIR A CALCANEOUS FRACTURE. THREE MONTHS POST-OPERATIVE, THE PT DEVELOPED AN INFECTION WITH CHRONIC DRAINAGE. THE DR CURETTED THE SURGICAL SITE AND REMOVED A PORTION OF THE DEVICE. THE PT HEALED AND IS PRESENTLY DOING WELL. THE DR DOES NOT RECALL THE PT'S NAME NOR DOES HE REMEMBER THE CAUSITIVE AGENT INVOLVED. THE DR STATED THAT LARGE FLAPS OF SKIN ARE PULLED BACK FOR THIS TYPE OF REPAIR PROCEDURE, AND A PLATE WITH SCREWS IS PLACED, THUS MAKING IT DIFFICULT TO DETERMINE AN EXACT CAUSE FOR INFECTION.