CrossFix® CM-9300

GUDID M543CM9300

CAYENNE MEDICAL, INC.

Fluted surgical drill bit, reusable

• Primary Device ID: M543CM9300
• NIH Device Record Key: 662297a2-f75c-4e75-806d-15db04479f0c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CrossFix®
• Version Model Number: CM-9300
• Catalog Number: CM-9300
• Company DUNS: 606719685
• Company Name: CAYENNE MEDICAL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M543CM9300 [Primary]

FDA Product Code

• HTW: Bit, Drill

Sterilization

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

[M543CM9300]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-04-08
• Device Publish Date: 2019-03-29

On-Brand Devices [CrossFix®]

• M543CM9300: CM-9300
• M543CM8000: CM-8000
• 00887868270031: CM-8000
• M543CM8002: CrossFix® All-Suture Meniscal Repair, curved
• M543CM8001: CrossFix® All-Suture Meniscal Repair, straight