Zavation CUSTOM CERVICAL DRILL

GUDID 00197157049935

CUSTOM CERVICAL DRILL

Zavation LLC

Manual surgical rotary handpiece, reusable

• Primary Device ID: 00197157049935
• NIH Device Record Key: a210a641-6168-4d37-a699-bf02bfd8bc97
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Zavation CUSTOM CERVICAL DRILL
• Version Model Number: ZAV-1372
• Company DUNS: 069472800
• Company Name: Zavation LLC
• 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: 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: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00197157049935 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112533

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00197157049935]

Moist Heat or Steam Sterilization

[00197157049935]

Moist Heat or Steam Sterilization

[00197157049935]

Moist Heat or Steam Sterilization

[00197157049935]

Moist Heat or Steam Sterilization

[00197157049935]

Moist Heat or Steam Sterilization

[00197157049935]

Moist Heat or Steam Sterilization

[00197157049935]

Moist Heat or Steam Sterilization

[00197157049935]

Moist Heat or Steam Sterilization

[00197157049935]

Moist Heat or Steam Sterilization

[00197157049935]

Moist Heat or Steam Sterilization

[00197157049935]

Moist Heat or Steam Sterilization

[00197157049935]

Moist Heat or Steam Sterilization

[00197157049935]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-01-21
• Device Publish Date: 2025-01-13

Devices Manufactured by Zavation LLC

• 00197157060183 - ZAVATION F3D CORPECTOMY: 2025-07-22 F3D CORPECTOMY - 14.5MM X 12MM X 61MM, 0 DEG
• 00197157060190 - ZAVATION F3D CORPECTOMY: 2025-07-22 F3D CORPECTOMY - 14.5MM X 12MM X 62MM, 0 DEG
• 00197157060206 - ZAVATION F3D CORPECTOMY: 2025-07-22 F3D CORPECTOMY - 14.5MM X 12MM X 63MM, 0 DEG
• 00197157060213 - ZAVATION F3D CORPECTOMY: 2025-07-22 F3D CORPECTOMY - 14.5MM X 12MM X 64MM, 0 DEG
• 00197157060220 - ZAVATION F3D CORPECTOMY: 2025-07-22 F3D CORPECTOMY - 14.5MM X 12MM X 65MM, 0 DEG
• 00197157060237 - ZAVATION F3D CORPECTOMY: 2025-07-22 F3D CORPECTOMY - 14.5MM X 12MM X 66MM, 0 DEG
• 00197157060244 - ZAVATION F3D CORPECTOMY: 2025-07-22 F3D CORPECTOMY - 14.5MM X 12MM X 67MM, 0 DEG
• 00197157060251 - ZAVATION F3D CORPECTOMY: 2025-07-22 F3D CORPECTOMY - 14.5MM X 12MM X 68MM, 0 DEG