Devices

Device Recall SpineTech

Model / Serial
Lot numbers P010900 and P010957
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
The instruments to be recalled are at 2 consignees in California and Mississippi. 21 units are with the firm''s sales representatives.
Product Description
Spine-Tech Ancillary Discectomy Instrument (Box Curette), Catalog Number 07.00254.001, in Spine-Tech Ancillary Discectomy Instrument Set, Catalog Number 07.00316.001.
Manufacturer
Sulzer Spine-Tech
1 Event
- Recall of Device Recall SpineTech

Manufacturer

Sulzer Spine-Tech

Manufacturer Address
Sulzer Spine-Tech, 7375 Bush Lake Road, Minneapolis MN 55439-2027
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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