FDA Adverse Event Other Summary report: N

ENCORE MODULAR HIP SYSTEM

MDR report key: 1552313 · Received December 3, 2009

Report

Report Number
1644408-2009-00573
Event Type
Other
Date Received
December 3, 2009
Date of Event
November 9, 2009
Report Date
November 9, 2009
Manufacturer
ENCORE MEDICAL, L.P.
Product Code
LPH
PMA / PMN Number
K955563
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SD, US
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

REVISION SURGERY - PT HIP DISLOCATING, 28MM HEAD DISLOCATING FROM FMP LINER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ENCORE MODULAR HIP SYSTEM FEMORAL HEAD, COCR LPH ENCORE MEDICAL, L.P. 275411

Patients

Seq Age Sex Outcome Treatment
1 79 YR Required Intervention 432-28-006/307771