Devices

Device Recall Hemostatic Bone Putty

Model / Serial
Part 10847A
Product Classification
General and Plastic Surgery Devices
Device Class
Unclassified
Implanted device?
Yes
Distribution
Distributed in the state of WI
Product Description
Hemostatic Bone Putty, for use as a water-soluble implant material and for use in the control of bleeding from bone surfaces.
Manufacturer
Synthes, Inc.
1 Event
- Recall of Device Recall Hemostatic Bone Putty

Manufacturer

Synthes, Inc.

Manufacturer Address
Synthes, Inc., 1302 Wrights Ln E, West Chester PA 19380-3417
Manufacturer Parent Company (2017)
Johnson & Johnson
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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