International Medical Devices Database

Manufacturer Address
Spine Smith Holdings, LLC, 93 Red River St, Austin TX 78701-4216
Manufacturer Parent Company (2017)
Spinesmith Holdings Llc
Source
USFDA
1 Event
- Recall of Device Recall VisuALIF

One device in the database

Device Recall VisuALIF

Model / Serial
Part Number: 0301-1410, Lot 53AR
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Distributed in FL.
Product Description
VisuALIF,System consisting of a 'U' shaped PEEK block in two footprint configurations, four heights and three lordosis angles., part number: 0301-1410. || Intended to be implanted via an open anterior approach.

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Disclaimer

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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Spine Smith Holdings, LLC

One device in the database

Device Recall VisuALIF