Escalate® PRO-1426

GUDID 10888857596634

Plate Holder

K2M, INC.

General internal orthopaedic fixation system implantation kit

• Primary Device ID: 10888857596634
• NIH Device Record Key: dda9cd5f-2577-44de-8a51-a6f3dc35a479
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Escalate®
• Version Model Number: PRO-1426
• Catalog Number: PRO-1426
• Company DUNS: 146060863
• Company Name: K2M, INC.
• 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(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10888857596634 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

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

[10888857596634]

Moist Heat or Steam Sterilization

[10888857596634]

Moist Heat or Steam Sterilization

[10888857596634]

Moist Heat or Steam Sterilization

[10888857596634]

Moist Heat or Steam Sterilization

[10888857596634]

Moist Heat or Steam Sterilization

[10888857596634]

Moist Heat or Steam Sterilization

[10888857596634]

Moist Heat or Steam Sterilization

[10888857596634]

Moist Heat or Steam Sterilization

[10888857596634]

Moist Heat or Steam Sterilization

[10888857596634]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-03-11
• Device Publish Date: 2026-03-03

Devices Manufactured by K2M, INC.

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• 10888857596993 - K2M General Instruments: 2026-04-01 Reverse Curette, Bayoneted
• 10888857580022 - LITe® Pedicle Based Retractor: 2026-03-12 Medial Blade 60 mm
• 10888857580039 - LITe® Pedicle Based Retractor: 2026-03-12 Medial Blade 70 mm
• 10888857580046 - LITe® Pedicle Based Retractor: 2026-03-12 Medial Blade 80 mm
• 10888857580053 - LITe® Pedicle Based Retractor: 2026-03-12 Medial Blade 90 mm
• 10888857580060 - LITe® Pedicle Based Retractor: 2026-03-12 Medial Blade 100 mm
• 10888857580077 - LITe® Pedicle Based Retractor: 2026-03-12 Medial Blade 110 mm