FDA Adverse Event Other Summary report: N

RSP SHOULDER

MDR report key: 1880566 · Received October 20, 2010

Report

Report Number
1644408-2010-00565
Event Type
Other
Date Received
October 20, 2010
Date of Event
October 6, 2010
Report Date
October 6, 2010
Manufacturer
ENCORE MEDICAL, L.P.
Product Code
KWS
PMA / PMN Number
K051075
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

REVISION SURGERY - NEUTRAL GLENOID HEAD WOULD NOT THREAD ON THE T-HANDLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 RSP SHOULDER NEUTRAL GLENOID HEAD KWS ENCORE MEDICAL, L.P. 457842

Patients

Seq Age Sex Outcome Treatment
1 57 YR Required Intervention