DOC 73100175

GUDID 10705034014678

DOC VENTRAL CERVICAL STABILIZATION SYSTEM FINLESS LOCKING PLATFORM

DEPUY SPINE, LLC

Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: 10705034014678
• NIH Device Record Key: 25601b1c-7524-496c-96e3-83f553a171df
• Commercial Distribution Discontinuation: 2019-11-30
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DOC
• Version Model Number: 73100175
• Catalog Number: 73100175
• Company DUNS: 107105876
• Company Name: DEPUY SPINE, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• 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(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705034014678 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K970955

FDA Product Code

• KWQ: APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Sterilization

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

[10705034014678]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-11-07
• Device Publish Date: 2015-09-24

On-Brand Devices [DOC]

• 10705034014678: DOC VENTRAL CERVICAL STABILIZATION SYSTEM FINLESS LOCKING PLATFORM
• 10705034014661: DOC VENTRAL CERVICAL STABILIZATION SYSTEM FINLESS NONLOCKING PLATFORM
• 10705034014654: DOC VENTRAL CERVICAL STABILIZATION SYSTEM DIVERGENT PLATFORM LOCKING
• 10705034014647: DOC VENTRAL CERVICAL STABILIZATION SYSTEM DIVERGENT PLATFORM NONLOCKING