MUST MINI OC pre-bent transition Rod

GUDID 07630040723596

MUST MINI OC pre-bent transition Rod 60° Ø3.5/4x 120mm (ste)

Medacta International SA

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• Primary Device ID: 07630040723596
• NIH Device Record Key: 07f660d9-69c6-416b-b944-9d50a6ae9c76
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MUST MINI OC pre-bent transition Rod
• Version Model Number: 03.75.848
• Company DUNS: 488227125
• Company Name: Medacta International SA
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07630040723596 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K182837

FDA Product Code

• NKG: Posterior Cervical Screw System

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-11-02
• Device Publish Date: 2021-10-25

On-Brand Devices [MUST MINI OC pre-bent transition Rod]

• 07630040723688: MUST MINI OC pre-bent transition Rod 75° Ø3.5/4x 200mm (ste)
• 07630040723671: MUST MINI OC pre-bent transition Rod 75° Ø3.5/4x 120mm (ste)
• 07630040723602: MUST MINI OC pre-bent transition Rod 60° Ø3.5/4x 200mm (ste)
• 07630040723596: MUST MINI OC pre-bent transition Rod 60° Ø3.5/4x 120mm (ste)
• 07630040723589: MUST MINI OC pre-bent transition Rod 45° Ø3.5/4x 200mm (ste)
• 07630040723572: MUST MINI OC pre-bent transition Rod 45° Ø3.5/4x 120mm (ste)