130 DEG FEM NECK FIX PLATE 1-HOLE 324-21301

GUDID 00810189110229

130 DEG FEM NECK FIX PLATE 1-HOLE

Osteocentric Technologies, Inc.

Orthopaedic fixation plate, non-bioabsorbable

• Primary Device ID: 00810189110229
• NIH Device Record Key: e2174eec-df5c-4ded-a7be-b52e5b06c37a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 130 DEG FEM NECK FIX PLATE 1-HOLE
• Version Model Number: 324-21301
• Catalog Number: 324-21301
• Company DUNS: 089645059
• Company Name: Osteocentric Technologies, Inc.
• 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: 1-800-969-0639
• Email: quality@osteocentric.com
• Phone: 1-800-969-0639
• Email: quality@osteocentric.com
• Phone: 1-800-969-0639
• Email: quality@osteocentric.com
• Phone: 1-800-969-0639
• Email: quality@osteocentric.com
• Phone: 1-800-969-0639
• Email: quality@osteocentric.com
• Phone: 1-800-969-0639
• Email: quality@osteocentric.com
• Phone: 1-800-969-0639
• Email: quality@osteocentric.com
• Phone: 1-800-969-0639
• Email: quality@osteocentric.com
• Phone: 1-800-969-0639
• Email: quality@osteocentric.com
• Phone: 1-800-969-0639
• Email: quality@osteocentric.com
• Phone: 1-800-969-0639
• Email: quality@osteocentric.com

Device Dimensions

• Length: 45 Millimeter
• Length: 45 Millimeter
• Length: 45 Millimeter
• Length: 45 Millimeter
• Length: 45 Millimeter
• Length: 45 Millimeter
• Length: 45 Millimeter
• Length: 45 Millimeter
• Length: 45 Millimeter
• Length: 45 Millimeter
• Length: 45 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810189110229 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K230764

FDA Product Code

• KTT: Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

Sterilization

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

[00810189110229]

Moist Heat or Steam Sterilization

[00810189110229]

Moist Heat or Steam Sterilization

[00810189110229]

Moist Heat or Steam Sterilization

[00810189110229]

Moist Heat or Steam Sterilization

[00810189110229]

Moist Heat or Steam Sterilization

[00810189110229]

Moist Heat or Steam Sterilization

[00810189110229]

Moist Heat or Steam Sterilization

[00810189110229]

Moist Heat or Steam Sterilization

[00810189110229]

Moist Heat or Steam Sterilization

[00810189110229]

Moist Heat or Steam Sterilization

[00810189110229]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-09-30
• Device Publish Date: 2025-09-22

Devices Manufactured by Osteocentric Technologies, Inc.

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• 00810074309974 - 11 X 80mm LAG FASTENER: 2025-09-30 11 X 80mm LAG FASTENER
• 00810074309981 - 11 X 85mm LAG FASTENER: 2025-09-30 11 X 85mm LAG FASTENER
• 00810074309998 - 11 X 90mm LAG FASTENER: 2025-09-30 11 X 90mm LAG FASTENER
• 00810189110007 - 11 X 95mm LAG FASTENER: 2025-09-30 11 X 95mm LAG FASTENER
• 00810189110014 - 11 X 100mm LAG FASTENER: 2025-09-30 11 X 100mm LAG FASTENER
• 00810189110021 - 11 X 105mm LAG FASTENER: 2025-09-30 11 X 105mm LAG FASTENER
• 00810189110038 - 11 X 110mm LAG FASTENER: 2025-09-30 11 X 110mm LAG FASTENER