NavLock

GUDID 00763000231521

NAVLOCK KIT 9736061K BLUE

MEDTRONIC NAVIGATION, INC.

Multi-purpose stereotactic surgery system

• Primary Device ID: 00763000231521
• NIH Device Record Key: f1b6e7d0-b9ef-40be-bbd4-a19664bb43ed
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NavLock
• Version Model Number: 9736061K
• Company DUNS: 835233107
• Company Name: MEDTRONIC NAVIGATION, INC.
• 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: false
• 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)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000231521 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K182104

FDA Product Code

• HAW: Neurological stereotaxic Instrument
• OLO: Orthopedic stereotaxic instrument

Sterilization

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

[00763000231521]

Moist Heat or Steam Sterilization

[00763000231521]

Moist Heat or Steam Sterilization

[00763000231521]

Moist Heat or Steam Sterilization

[00763000231521]

Moist Heat or Steam Sterilization

[00763000231521]

Moist Heat or Steam Sterilization

[00763000231521]

Moist Heat or Steam Sterilization

[00763000231521]

Moist Heat or Steam Sterilization

[00763000231521]

Moist Heat or Steam Sterilization

[00763000231521]

Moist Heat or Steam Sterilization

[00763000231521]

Moist Heat or Steam Sterilization

[00763000231521]

Moist Heat or Steam Sterilization

[00763000231521]

Moist Heat or Steam Sterilization

[00763000231521]

Moist Heat or Steam Sterilization

[00763000231521]

Moist Heat or Steam Sterilization

[00763000231521]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-06-29
• Device Publish Date: 2019-01-19

On-Brand Devices [NavLock]

• 00643169101968: TRACKER 9734734 NavLock UNIVERSAL GREEN
• 00643169089600: HANDLE 9733734 RATCHETING QC SM STRGHT
• 00763000231835: NAVLOCK KIT 9736060K BLACK
• 00763000231521: NAVLOCK KIT 9736061K BLUE
• 00763000123185: NAVLOCK 9736061 BLUE
• 00763000123178: NAVLOCK 9736060 BLACK
• 00763000054465: HANDLE 9733734 RATCHETING QC SM STRGHT
• 00763000054489: TRACKER 9734734 NavLock UNIVERSAL GREEN