Devices

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
1 Event
- Recall of Device Recall Stride Femoral Component

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 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

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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