Silverbolt/Mainframe Instruments

GUDID 00840996163569

SILVERBOLT,TAP, W REAMER TIP, 6.0

Choice Spine, LP

Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: 00840996163569
• NIH Device Record Key: 3f8e82dc-26f6-4a31-b007-203d9eed1231
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Silverbolt/Mainframe Instruments
• Version Model Number: 200-9265
• Company DUNS: 078293017
• Company Name: Choice Spine, LP
• 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(865)246-3333
• Email: info@choicespine.net

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840996163569 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00840996163569]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-09-11

On-Brand Devices [Silverbolt/Mainframe Instruments]

• 00840996169233: S'BOLT,DRIVER,POLY,SOLID,MAINFRAME
• 00840996169226: S'BOLT,CANN,DR,POLY,MAINFRAME
• 00840996163576: SILVERBOLT,TAP, W REAMER TIP, 7.0
• 00840996163569: SILVERBOLT,TAP, W REAMER TIP, 6.0
• 00840996157469: SILVERBOLT,DRIVER, X-15
• 00840996156615: SILVERBOLT,ROD REDUCER
• 00840996187398: SILVERBOLT,TISSUE SPLIT BLD,(2)
• 00840996181297: SILVERBOLT, TAP, W REAMER, 5.5