M.U.S.T. Cross Connectors

GUDID 07630030839788

MUST LINK 40-50

Medacta International SA

Bone-screw internal spinal fixation system

• Primary Device ID: 07630030839788
• NIH Device Record Key: 153f6c3d-50b7-4c45-84a3-5e77448026a5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: M.U.S.T. Cross Connectors
• Version Model Number: 03.56.040
• 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	07630030839788 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132878

FDA Product Code

• NKB: Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2014-09-17

On-Brand Devices [M.U.S.T. Cross Connectors]

• 07630030839801: MUST LINK 64-98
• 07630030839795: MUST LINK 48-66
• 07630030839788: MUST LINK 40-50
• 07630030839771: MUST LINK 35-42