MUSTmini OC pre-bent Rod

GUDID 07630030865114

MUST MINI OC pre-bent Rod 45° Ø3.5x 200mm (ste)

Medacta International SA

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• Primary Device ID: 07630030865114
• NIH Device Record Key: d653171d-2a25-4757-ae44-31793e5b035e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MUSTmini OC pre-bent Rod
• Version Model Number: 03.75.621
• 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	07630030865114 [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 [MUSTmini OC pre-bent Rod]

• 07630030865152: MUST MINI OC pre-bent Rod 75° Ø3.5x 200mm (ste)
• 07630030865145: MUST MINI OC pre-bent Rod 75° Ø3.5x 120mm (ste)
• 07630030865138: MUST MINI OC pre-bent Rod 60° Ø3.5x 200mm (ste)
• 07630030865121: MUST MINI OC pre-bent Rod 60° Ø3.5x 120mm (ste)
• 07630030865114: MUST MINI OC pre-bent Rod 45° Ø3.5x 200mm (ste)
• 07630030865107: MUST MINI OC pre-bent Rod 45° Ø3.5x 120mm (ste)