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Device Recall Stride Femoral Component
Model / Serial
Lot C785231, Exp 5-2015
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
US Nationwide Distribution in the states of CA, PA, and TX
Product Description
Stride Femoral Component Size 2, PFSI-00053, Right Lateral /Left Medial. Unicondylar Knee prosthesis.
Manufacturer
Blue Belt Technologies MN
1 Event
Recall of Device Recall Stride Femoral Component
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Manufacturer
Blue Belt Technologies MN
Manufacturer Address
Blue Belt Technologies MN, 2905 Northwest Blvd Ste 40, Plymouth MN 55441-2673
Source
USFDA
One device with a similar name
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Device Recall Stride Femoral Component
Model / Serial
Lot C785241, Exp 4-2015
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
US Nationwide Distribution in the states of CA, PA, and TX
Product Description
Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral. Unicondylar Knee prosthesis.
Manufacturer
Blue Belt Technologies MN
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