Devices

Device Recall DRP SCREW

Model / Serial
Lot number 1602134
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Worldwide Distribution - US TN only and Internationally to France and Switzerland
Product Description
NEOVIEW(R) SCREWS SET, REF W27 ST900, STERILE R || The NEOVIEW¿ Plating System is intended for fixation of intra-articular and extraarticular fractures of the distal radius and reconstruction of the distal radius
Manufacturer
In2Bones, SAS
1 Event
- Recall of Device Recall DRP SCREW

Manufacturer

In2Bones, SAS

Manufacturer Address
In2Bones, SAS, 28 Chemin du petit Bois, Ecully France
Manufacturer Parent Company (2017)
In2Bones SAS
Source
USFDA

2 devices with a similar name

Learn more about the data here

Device Recall DRP SCREW

Model / Serial
Lot Numbers: a) 1602064, b) 1606067
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Worldwide Distribution - US TN only and Internationally to France and Switzerland
Product Description
SCREW 02.7-12MM LOCKING, REF W27 ST112: a) DRP, b) NEO, In2Bones, 28 chemin du petit bois, 69130 Ecully - France || The NEOVIEW¿ Plating System is intended for fixation of intra-articular and extraarticular fractures of the distal radius and reconstruction of the distal radius
Manufacturer
In2Bones, SAS

Device Recall DRP SCREW

Model / Serial
Lot Numbers: 1604154, 1605083, 1606068
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Worldwide Distribution - US TN only and Internationally to France and Switzerland
Product Description
NEO SCREW 02.7-14MM LOCKING, REF W27 ST114, In2Bones, 28 chemin du petit bois, 69130 Ecully - France || The NEOVIEW¿ Plating System is intended for fixation of intra-articular and extraarticular fractures of the distal radius and reconstruction of the distal radius
Manufacturer
In2Bones, SAS

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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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