General Instruments ST3-000000

GUDID 10889981273736

Universal Lid, 20 X 10

SEASPINE ORTHOPEDICS CORPORATION

Instrument tray, reusable

• Primary Device ID: 10889981273736
• NIH Device Record Key: fe8f77ce-e22e-47ae-9a7a-acc0e7a6113d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: General Instruments
• Version Model Number: ST3-000000
• Catalog Number: ST3-000000
• Company DUNS: 079840876
• Company Name: SEASPINE ORTHOPEDICS 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: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10889981273736 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211606

FDA Product Code

• NKB: Thoracolumbosacral pedicle screw system

Sterilization

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

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

[10889981273736]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-09-02
• Device Publish Date: 2021-08-25

Devices Manufactured by SEASPINE ORTHOPEDICS CORPORATION

• 10889981425753 - Reef L: 2026-02-09 LATERAL IMPLANT, 23mm X 8mm X 50mm, 15°
• 10889981426248 - Reef L: 2026-02-09 LATERAL IMPLANT, 18mm X 8mm X 50mm, 15°
• 10889981426293 - Reef L: 2026-02-09 LATERAL IMPLANT, 23mm X 8mm X 40mm, 15°
• 10889981426422 - Reef L: 2026-02-09 LATERAL IMPLANT, 23mm X 8mm X 55mm, 15°
• 10889981426521 - Reef L: 2026-02-09 LATERAL IMPLANT, 18mm X 8mm X 60mm, 15°
• 10889981426552 - Reef L: 2026-02-09 LATERAL IMPLANT, 18mm X 8mm X 55mm, 15°
• 10889981426590 - Reef L: 2026-02-09 LATERAL IMPLANT, 23mm X 8mm X 60mm, 15°
• 10889981426675 - Reef L: 2026-02-09 LATERAL IMPLANT, 18mm X 8mm X 45mm, 15°