Devices

Device Recall Aesculap S4 Cervical (S4C) Revision Instruments (FW099R and FW101R)

Model / Serial
All distributed lot numbers and serial numbers
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide distribution, including the states of CA, CO, IL, LA, NV, OH, and TX .
Product Description
S4 Cervical (S4C) Revision Instruments (FW099R and FW101R). The S4C Revision Instruments assist in the removal of an occipital cervical screw during revision surgery.
Manufacturer
Aesculap Implant Systems LLC
1 Event
- Recall of Device Recall Aesculap S4 Cervical (S4C) Revision Instruments (FW099R and FW101R)

Manufacturer

Aesculap Implant Systems LLC

Manufacturer Address
Aesculap Implant Systems LLC, 3773 Corporate Pkwy, Center Valley PA 18034-8217
Manufacturer Parent Company (2017)
Ludwig G. Braun Gmbh U. Co. Kg
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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