289215112

GUDID 10705034548234

ATP/Lateral Discectomy Instruments Lateral Angled Cobb Elevator Left, Navigable Angled 20mm

Medos International Sàrl

Bone lever/elevator, reusable

• Primary Device ID: 10705034548234
• NIH Device Record Key: 07fda4fe-3d53-4588-b162-5e0af7cd1c14
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 289215112
• Catalog Number: 289215112
• Company DUNS: 482661753
• Company Name: Medos International Sàrl
• 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: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705034548234 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K212756

FDA Product Code

• OLO: Orthopedic stereotaxic instrument

Sterilization

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

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

[10705034548234]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-08-17
• Device Publish Date: 2022-08-09

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• 10705034587622 - TRIALTIS: 2025-08-12 TRIALTIS Spine System Closed Lateral Connector Adjustable ø5.5-6.35mm to 6mm x 40mm
• 10705034587639 - TRIALTIS: 2025-08-12 TRIALTIS Spine System Closed Lateral Connector Adjustable ø5.5-6.35mm to 6mm x 60mm
• 10705034601342 - TRIALTIS: 2025-08-12 TRIALTIS Spine System Closed Lateral Connector Adjustable,Flanged ø5.5-6.35mm to 6mm x 20mm
• 10705034601366 - TRIALTIS: 2025-08-12 TRIALTIS Spine System Closed Lateral Connector Adjustable, Flanged ø5.5-6.35mm to 6mm x 40mm
• 10705034601380 - TRIALTIS: 2025-08-12 TRIALTIS Spine System Closed Lateral Connector Adjustable, Flanged ø5.5-6.35mm to 6mm x 60mm
• 10705034604589 - TRIALTIS: 2025-08-12 TRIALTIS Spine System Side by Side Connector, Long Open / Snap On ø5.5-6mm to 5.5-6.35mm
• 10705034604602 - TRIALTIS: 2025-08-12 TRIALTIS Spine System Side by Side Connector,Short Open / Snap On ø5.5-6mm to 5.5-6.35mm