Valeo Interbody Fusion System 91.013.3309

GUDID M555910133309

PL Trial 9X25, 0 Degree, Integral Shaft, 9mm

AMEDICA CORPORATION

Internal spinal fixation procedure kit, single-use

• Primary Device ID: M555910133309
• NIH Device Record Key: f43b6dc8-6bc7-4bcc-949d-781b59a4af3d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Valeo Interbody Fusion System
• Version Model Number: A
• Catalog Number: 91.013.3309
• Company DUNS: 028629553
• Company Name: AMEDICA CORPORATION
• 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: 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: 801-839-3500
• Email: customerservice@amedica.com

Device Dimensions

• Height: 9 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M555910133309 [Primary]

FDA Product Code

• ODP: Intervertebral Fusion Device With Bone Graft, Cervical

Sterilization

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

[M555910133309]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-06-07
• Device Publish Date: 2017-12-29

On-Brand Devices [Valeo Interbody Fusion System]

• M555910133309: PL Trial 9X25, 0 Degree, Integral Shaft, 9mm
• M555910023108: Trial 16x12, 0°, 8mm
• M555123011513: Valeo II PL 11x23 5°, 13mm
• M555110165123: Valeo II AL, 36x28, 12°, 13mm
• M555110091005: Valeo C 16x12, 0°, 5mm with Alternate Texturing