MEDPOR CONTAIN IMPLANT 81065

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2011-07-01 for MEDPOR CONTAIN IMPLANT 81065 manufactured by Stryker Craniomaxillofacial Georgia.

Event Text Entries

[19754089] The device history records were reviewed and all processes and test criteria were within the (b)(4) implant specification. Device not returned.
Patient Sequence No: 1, Text Type: N, H10


[19843279] In (b)(6) 2010, dr. (b)(6) placed a bone graft, bmp/acs, regene form 0. 5cc block, covered with bmp/acs, held in place with 0. 45 mm (b)(4) contain sheet implant , again covered with layer of bmp/acs, and primary closure, in the anterior maxilla area of teeth 8-10. Postoperatively dr. (b)(6) stated that he observed exposure of the occlusal portion of the graft. Radiographically it appears the graft is not forming bone and there appears to be bone loss associated with the mesial aspect of #10.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1057129-2011-00018
MDR Report Key2147899
Report Source05,07
Date Received2011-07-01
Date of Report2011-07-01
Date Mfgr Received2011-06-10
Device Manufacturer Date2010-03-31
Date Added to Maude2011-07-05
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMR. JEFF WILLIAMS
Manufacturer Street15 DART ROAD
Manufacturer CityNEWNAN GA 302651017
Manufacturer CountryUS
Manufacturer Postal302651017
Manufacturer Phone7702544400
Manufacturer G1STRYKER CRANIOMAXILLOFACIAL GEORGIA
Manufacturer Street15 DART ROAD
Manufacturer CityNEWNAN GA 30265101
Manufacturer CountryUS
Manufacturer Postal Code30265 1017
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMEDPOR CONTAIN IMPLANT
Generic NameIMPLANT
Product CodeNPK
Date Received2011-07-01
Model NumberNA
Catalog Number81065
Lot NumberF048C03
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER CRANIOMAXILLOFACIAL GEORGIA
Manufacturer Address15 DART ROAD NEWNAN GA 30265101 US 30265 1017


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2011-07-01

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