292801

GUDID 20887587029693

2.0MM KIRSCHNER WIRE W/CALIB W/15MM THRD-TROCAR POINT-150MM

SYNTHES (U.S.A.) LP

Implantable craniofacial bone distractor

• Primary Device ID: 20887587029693
• NIH Device Record Key: 464a365a-f070-49eb-8f10-e154c01ebe38
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 292.801
• Catalog Number: 292801
• Company DUNS: 832637081
• Company Name: SYNTHES (U.S.A.) LP
• Device Count: 10
• 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)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	20887587029693 [Primary]
GS1	80887587029695 [Unit of Use]
HIBCC	H9802928010 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K981362

FDA Product Code

• DZL: SCREW, FIXATION, INTRAOSSEOUS

Sterilization

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

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

[20887587029693]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-09-23
• Device Publish Date: 2015-09-14

Devices Manufactured by SYNTHES (U.S.A.) LP

• 10886982297280 - NA: 2024-09-11 SCHANZ PIN REMOVAL TOOL
• H9814871830 - Click'X: 2024-09-11 7.0MM TI CLICK'X® MONOAXIAL PEDICLE SCREW 90MM THRD LENGTH
• H9812982060 - NA: 2024-07-24 ANGLED LAMINA HOOK/ DUAL-OPENING SIDE
• H6792042280 - NA: 2024-07-24 3.5MM SHAFT SCREW 28MM
• H6792042320 - NA: 2024-07-24 3.5MM SHAFT SCREW 32MM
• H6792042340 - NA: 2024-07-24 3.5MM SHAFT SCREW 34MM
• H6792042360 - NA: 2024-07-24 3.5MM SHAFT SCREW 36MM
• H6792042380 - NA: 2024-07-24 3.5MM SHAFT SCREW 38MM