CASSATT

GUDID 00841732131606

CASSATT Rasp, W12 x L30, H8

CTL Medical Corporation

Internal spinal fixation procedure kit, reusable

• Primary Device ID: 00841732131606
• NIH Device Record Key: 2b866a63-be3b-41ac-bb18-2c9f9a78e1c0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CASSATT
• Version Model Number: 133.7418
• Company DUNS: 080138504
• Company Name: CTL Medical Corporation
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841732131606 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211785

FDA Product Code

• OUR: Sacroiliac Joint Fixation

Sterilization

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

[00841732131606]

Moist Heat or Steam Sterilization

[00841732131606]

Moist Heat or Steam Sterilization

[00841732131606]

Moist Heat or Steam Sterilization

[00841732131606]

Moist Heat or Steam Sterilization

[00841732131606]

Moist Heat or Steam Sterilization

[00841732131606]

Moist Heat or Steam Sterilization

[00841732131606]

Moist Heat or Steam Sterilization

[00841732131606]

Moist Heat or Steam Sterilization

[00841732131606]

Moist Heat or Steam Sterilization

[00841732131606]

Moist Heat or Steam Sterilization

[00841732131606]

Moist Heat or Steam Sterilization

[00841732131606]

Moist Heat or Steam Sterilization

[00841732131606]

Moist Heat or Steam Sterilization

[00841732131606]

Moist Heat or Steam Sterilization

[00841732131606]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-04-01
• Device Publish Date: 2025-03-24

On-Brand Devices [CASSATT]

• 00841732167315: Cassatt Implants Screws-Cannulated 11.5 & 12.5
• 00841732131606: CASSATT Rasp, W12 x L30, H8
• 00841732129603: CASSATT Trial, W11 x L24 mm, H6 mm