60501129

GUDID 07612334263544

MATRIXSTERNUM SCREW MODULE

Synthes GmbH

Surgical instrument/implant rack

• Primary Device ID: 07612334263544
• NIH Device Record Key: ed70c530-141d-495e-9c0c-bd9712e82ada
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 60.501.129
• Catalog Number: 60501129
• Company DUNS: 486711679
• Company Name: Synthes GmbH
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07612334263544 [Direct Marking]
GS1	10887587078151 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K233967

FDA Product Code

• HRS: Plate, fixation, bone

Sterilization

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

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

[07612334263544]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-08-29
• Device Publish Date: 2024-08-21

Devices Manufactured by Synthes GmbH

• 10886982350435 - NA: 2026-02-19 HALF BENNETT SMALL/LEFT
• 10886982350442 - NA: 2026-02-19 HALF BENNETT SMALL/RIGHT
• 10886982350459 - NA: 2026-02-19 HALF BENNETT LARGE/LEFT
• 10886982350466 - NA: 2026-02-19 HALF BENNETT LARGE/RIGHT
• 10886982351579 - NA: 2026-02-19 SHOULDER HOOK 2.2 MM TIP / 235 MM LENGTH
• 10886982351661 - NA: 2026-02-19 T-HANDLE AO CONNECTOR
• 10886982351678 - NA: 2026-02-19 T-HANDLE LARGE AO CONNECTOR
• 10886982361288 - NA: 2026-02-19 5MM AWL, QC