Medium Flat Osteotome Blade 2500-10-751

GUDID 00847538009378

Medium Flat Osteotome Blade

SYMMETRY MEDICAL INC.

Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome

• Primary Device ID: 00847538009378
• NIH Device Record Key: a8ea3491-d5ca-4d16-a984-fda7d51764bf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medium Flat Osteotome Blade
• Version Model Number: 11-130-502
• Catalog Number: 2500-10-751
• Company DUNS: 079881212
• Company Name: SYMMETRY 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	00847538009378 [Primary]

FDA Product Code

• GFI: Osteotome, Manual

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-02
• Device Publish Date: 2023-09-22

On-Brand Devices [Medium Flat Osteotome Blade]

• 00847538009361: Medium Flat Osteotome Blade
• 00847538009378: Medium Flat Osteotome Blade