Juliet PO DYN-PX 22 10-S

GUDID 07640151086008

Lumbar Posterior Cage Extra Lordotic

SpineArt SA

Polymeric spinal fusion cage, sterile

• Primary Device ID: 07640151086008
• NIH Device Record Key: 16a58799-50c2-49ca-8163-9a287e876655
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Juliet PO
• Version Model Number: DYN-PX 22 10-S
• Catalog Number: DYN-PX 22 10-S
• Company DUNS: 483016148
• Company Name: SpineArt SA
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter
• Angle: 12 degree
• Height: 10 Millimeter
• Depth: 22 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640151086008 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142277

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-02-11
• Device Publish Date: 2015-10-21

On-Brand Devices [Juliet PO]

• 07640151086022: Lumbar Posterior Cage Extra Lordotic
• 07640151086015: Lumbar Posterior Cage Extra Lordotic
• 07640151086008: Lumbar Posterior Cage Extra Lordotic
• 07640151085995: Lumbar Posterior Cage Extra Lordotic