PRO-SPEC 03.845.012

GUDID 00810112599312

EVANS OSTEOTOMY TRIAL 18MMX12MM

CROSSROADS EXTREMITY SYSTEMS

Surgical implant template, reusable

• Primary Device ID: 00810112599312
• NIH Device Record Key: 5ca8c015-3aba-417d-81ff-22d9e003a0ab
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRO-SPEC
• Version Model Number: EVANS OSTEOTOMY TRIAL 18MMX12MM
• Catalog Number: 03.845.012
• Company DUNS: 058864308
• Company Name: CROSSROADS EXTREMITY SYSTEMS
• 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
GS1	00810112599312 [Primary]

FDA Product Code

• HWT: Template

Sterilization

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

[00810112599312]

Moist Heat or Steam Sterilization

[00810112599312]

Moist Heat or Steam Sterilization

[00810112599312]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-03-12
• Device Publish Date: 2025-03-04

On-Brand Devices [PRO-SPEC]

• 00810112599336: EVANS OSTEOTOMY TRIAL 20MMX8MM
• 00810112599329: EVANS OSTEOTOMY TRIAL 20MMX6MM
• 00810112599312: EVANS OSTEOTOMY TRIAL 18MMX12MM
• 00810112599305: EVANS OSTEOTOMY TRIAL 18MMX10MM
• 00810112599299: EVANS OSTEOTOMY TRIAL 18MMX8MM
• 00810112599282: EVANS OSTEOTOMY TRIAL 18MMX6MM