MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,08 report with the FDA on 2006-05-11 for OSTEOFIL ICM MOLDABLE STRIP 002390 manufactured by Regeneration Technologies, Inc..
[448918]
The pt underwent spinal fusion in 2005. The pt developed an infection approx 5 wks post operatively.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3002719998-2006-00002 |
MDR Report Key | 712820 |
Report Source | 05,08 |
Date Received | 2006-05-11 |
Date of Report | 2006-05-10 |
Date of Event | 2006-01-21 |
Date Mfgr Received | 2006-02-22 |
Device Manufacturer Date | 2001-09-01 |
Date Added to Maude | 2006-05-15 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 0 |
Manufacturer Contact | AUDRA MCCONNELL |
Manufacturer Street | 11621 RESEARCH CIRCLE P. O. BOX 2650 |
Manufacturer City | ALACHUA FL 32616 |
Manufacturer Country | US |
Manufacturer Postal | 32616 |
Manufacturer Phone | 3864188888 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | OSTEOFIL ICM MOLDABLE STRIP |
Generic Name | ALLOGRAFT PASTE |
Product Code | LMO |
Date Received | 2006-05-11 |
Model Number | 002390 |
Catalog Number | 002390 |
Lot Number | 101044025 |
ID Number | * |
Device Expiration Date | 2010-09-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Implant Flag | Y |
Date Removed | * |
Device Sequence No | 1 |
Device Event Key | 701888 |
Manufacturer | REGENERATION TECHNOLOGIES, INC. |
Manufacturer Address | * ALACHUA FL * US |
Baseline Brand Name | OSTEOFIL ICM MOLDABLE STRIP |
Baseline Generic Name | ALLOGRAFT BONE PASTE |
Baseline Model No | 002390 |
Baseline Catalog No | 002390 |
Baseline ID | NA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2006-05-11 |