Devices

Device Recall TiBond

Model / Serial
All revisions
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution
Product Description
Ti-Bond Marketing Literature/Labeling, Catalog No. LT10000, MP-14000 || This device is intended to be used with autogenous bone graft. Patients must have undergone a regimen of at least six (6) months non-operative treatment prior to being treated with this device.
Manufacturer
Spinal Elements, Inc
1 Event
- Recall of Device Recall TiBond

Manufacturer

Spinal Elements, Inc

Manufacturer Address
Spinal Elements, Inc, 3115 Melrose Dr, Suite 200, Carlsbad CA 92010-6690
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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