M.U.S.T. Lateral connector

GUDID 07630030839832

Lateral connector 60mm

Medacta International SA

Trans-facet-screw internal spinal fixation system, sterile

• Primary Device ID: 07630030839832
• NIH Device Record Key: 127e1aa8-8220-42d3-920f-202224bf96bc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: M.U.S.T. Lateral connector
• Version Model Number: 03.56.102
• 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	07630030839832 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162061

FDA Product Code

• KWP: Appliance, Fixation, Spinal Interlaminal

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-02-09

On-Brand Devices [M.U.S.T. Lateral connector]

• 07630030839863: Unsterile - Lateral connector 60mm
• 07630030839856: Unsterile - Lateral connector 40mm
• 07630030839849: Unsterile - Lateral connector 20mm
• 07630030839832: Lateral connector 60mm
• 07630030839825: Lateral connector 40mm
• 07630030839818: Lateral connector 20mm