443174

GUDID H9814431740

2.0MM TI MINIPLATE-DOUBLE BEND 27MM/4MM SPACING

Synthes GmbH

Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: H9814431740
• NIH Device Record Key: 7b214b00-8aa3-4b03-bf10-d8f70d9b4643
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 443.174
• Catalog Number: 443174
• 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: 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
• 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	10705034779935 [Primary]
HIBCC	H9814431740 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K032534

FDA Product Code

• NQW: ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL

Sterilization

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

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

[H9814431740]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2022-04-27
• Device Publish Date: 2015-09-14

Devices Manufactured by Synthes GmbH

• 07612334260079 - KINCISE: 2024-11-08 KINCISE(TM) SYSTEM SURGICAL HANDPIECE CASE
• 07612334268587 - KINCISE: 2024-11-08 KINCISE(TM) SYSTEM STERILIZATION CASE LID
• 07612334268679 - KINCISE: 2024-11-08 KINCISE(TM) SYSTEM PRIMARY HIP ADAPTER CASE
• 07612334268563 - KINCISE: 2024-11-04 KINCISE™ System Automated Surgical Handpiece V2
• 07612334268570 - KINCISE: 2024-11-04 KINCISE™ System Lithium-ion Battery
• 07612334268594 - KINCISE: 2024-11-04 KINCISE™ System Primary Hip PINNACLE™ Straight Shell/Liner Impactor - Long
• 07612334268600 - KINCISE: 2024-11-04 KINCISE™ System Primary Hip PINNACLE™ Offset Shell/Liner Impactor
• 07612334268617 - KINCISE: 2024-11-04 KINCISE™ System Primary Hip PINNACLE™ Inclination Guide