FDA Adverse Event Other Summary report: N

MIDFOOT M1 - C1 SMALL PLATE - LEFT

MDR report key: 1943816 · Received December 21, 2010

Report

Report Number
9615741-2010-00067
Event Type
Other
Date Received
December 21, 2010
Date of Event
November 15, 2010
Report Date
December 21, 2010
Manufacturer
NEWDEAL
Product Code
HRS
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TO DATE, THE DEVICE INVOLVED IN THE REPORTED INCIDENT HAS NOT BEEN RECEIVED FOR EVAL. AN INVESTIGATION HAS BEEN INITIATED BASED UPON THE REPORTED INFO.

Description of Event or Problem · 1

THE REPORTER STATED THAT THE PT HAD A SURGICAL PROCEDURE ON (B)(6) 2010, USING AN ADVANSYS MID FOOT PLATING SYS: MEDIAL LISFRANC PLATE. ON (B)(6) 2010, THE PT HAD A SECOND SURGICAL PROCEDURE TO PERFORM A TENDON PLASTY. INTEGRA HAS REQUESTED ADDITIONAL CLINICAL INFO.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MIDFOOT M1 - C1 SMALL PLATE - LEFT NA HRS NEWDEAL

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention