SpineSTAR® STR-0510L/B

GUDID 00884450488553

Merit Medical Systems, Inc.

Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar

• Primary Device ID: 00884450488553
• NIH Device Record Key: 566bdfc0-baf9-4860-abef-15242bbeb04d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SpineSTAR®
• Version Model Number: 10884450488550
• Catalog Number: STR-0510L/B
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 75
• 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: true
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450488553 [Unit of Use]
GS1	10884450488550 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K091310

FDA Product Code

• GEI: Electrosurgical, cutting & coagulation & accessories

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: 2022-10-13
• Device Publish Date: 2022-10-05

On-Brand Devices [SpineSTAR®]

• 10884450296094: 00884450296097
• 10884450296087: 00884450296080
• 10884450296001: 00884450296004
• 10884450296032: 00884450296035
• 00884450488553: 10884450488550
• 10884450488321: 00884450488324
• 00884450488560: 10884450488567