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 |