LIF Revision Instruments

GUDID 00190376556017

LIF Revision Hook, Bayonetted 10mm

ALPHATEC SPINE, INC.

Orthopaedic inorganic implant inserter/extractor, reusable

• Primary Device ID: 00190376556017
• NIH Device Record Key: b4d61470-2403-42ef-a329-b92efa1ba22c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIF Revision Instruments
• Version Model Number: 254-06-010-10
• Company DUNS: 602465783
• Company Name: ALPHATEC SPINE, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com
• Phone: +1(760)431-9286
• Email: Regulatory@alphatecspine.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00190376556017 [Primary]

FDA Product Code

• GDI: DISSECTOR, SURGICAL, GENERAL & PLASTIC SURGERY

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

[00190376556017]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-15
• Device Publish Date: 2024-11-07

On-Brand Devices [LIF Revision Instruments]

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• 00190376556109: Offset Osteophyter
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• 00190376556086: LIF, Pituitary Rongeur, Bayonetted, 7mm
• 00190376556079: LIF, Pituitary Rongeur, Bayonetted, 6mm
• 00190376556062: LIF, Pituitary Rongeur, Bayonetted, 5mm
• 00190376556055: LIF, Pituitary Rongeur, Bayonetted, 4mm
• 00190376556048: LIF, Pituitary Rongeur, Bayonetted, 3mm
• 00190376556031: LIF, Pituitary Rongeur, Bayonetted, 2mm
• 00190376556024: LIF Implant Removal Rongeur
• 00190376556017: LIF Revision Hook, Bayonetted 10mm
• 00190376556000: LIF Revision Hook, Bayonetted 7mm
• 00190376555997: LIF Revision Pick, 7mm
• 00190376555980: LIF Revision Pick, 5mm
• 00190376555973: LIF Revision Hook, Straight 10mm
• 00190376555966: LIF Revision Hook, Straight 7mm
• 00190376555959: Ti Implant Threaded Removal Tool, L
• 00190376555942: Ti Implant Threaded Removal Tool, M
• 00190376555935: Ti Implant Threaded Removal Tool, S
• 00190376555928: PEEK Implant Threaded Removal Tool, L
• 00190376555911: PEEK Implant Threaded Removal Tool, M
• 00190376555904: PEEK Implant Threaded Removal Tool, S
• 00190376555898: LIF Revision Drill
• 00190376555881: LIF Revision Drill Guide