Devices

Device Recall ORTHOFIX, Connector System, LARGE SET SCREW

Model / Serial
UDI 18257200125364, Lot Numbers: O01 and O02
Product Classification
Orthopedic Devices
Device Class
Unclassified
Implanted device?
Yes
Distribution
US
Product Description
ORTHOFIX, Connector System, LARGE SET SCREW, REF 79-2002
Manufacturer
Orthofix, Inc
1 Event
- Recall of Device Recall ORTHOFIX, Connector System, LARGE SET SCREW

Manufacturer

Orthofix, Inc

Manufacturer Address
Orthofix, Inc, 3451 Plano Pkwy, Lewisville TX 75056-9453
Manufacturer Parent Company (2017)
Orthofix International Nv
Source
USFDA

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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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