Devices

Device Recall Leucadia Autolok" Polyaxial Pedicle Screw System

Model / Serial
83010 85001 85002 83005-30 83005-35 83005-40 83005-45 83005-50 83006-30 83006-35 83006-40 83006-45 83006-50 83006-55 83006-60 83007-30 83007-35 83007-40 83007-45 83007-50 83007-55 83008-30 83008-35 83008-40 83008-45 83008-50 83008-55 83008-80 82001-1 Catalog Numbers: LA-HSS0010 LA-HDOO01 LA-CTOO02 LA-PS0530 LA-PS0535 LA-PS0540 LA-PS0545 LA-PS0550 LA-PS0630 LA-PS0635 LA-PS0640 LA-PS0645 LA-PS0650 LA-PS0655 LA-PS0660 LA-PS0730 LA-PS0735 LA-PS0740 LA-PS0745 LA-PS0750 LA-PS0755 LA-PS0830 LA-PS0835 LA-PS0840 LA-PS0845 LA-PS0850 LA-PS0855 LA-PS0880 LA-SOO01 Lots Affected: All
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution.
Product Description
Leucadia Autolok" Polyaxial Pedicle Screw System. || Intended to help provide correction, immobilization and stabilization of spinal segments.
Manufacturer
Alphatec Spine, Inc.
1 Event
- Recall of Device Recall Leucadia Autolok" Polyaxial Pedicle Screw System

Manufacturer

Alphatec Spine, Inc.

Manufacturer Address
Alphatec Spine, Inc., 5818 El Camino Real, Carlsbad CA 92008-8816
Manufacturer Parent Company (2017)
Alphatec Holdings Inc.
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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