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FDA 510(k)

Visualase V2 MRI-guided Laser Ablation System (9736422)

K-Number: K250307 · 2025-05-29

Decision Date2025-05-29
Product CodeONO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Visualase V2 MRI-guided Laser Ablation System (9736422) is a medical device manufactured by Medtronic Navigation. It received FDA 510(k) clearance on 2025-05-29 under approval number K250307. The device is classified under product code ONO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Visualase V2 MRI-guided Laser Ablation System (9736422)?

Visualase V2 MRI-guided Laser Ablation System (9736422) is a medical device that received FDA 510(k) clearance on 2025-05-29. It is manufactured by Medtronic Navigation. The 510(k) number is K250307.

When was Visualase V2 MRI-guided Laser Ablation System (9736422) approved by the FDA?

Visualase V2 MRI-guided Laser Ablation System (9736422) received FDA 510(k) clearance on 2025-05-29, under approval number K250307.

What company makes Visualase V2 MRI-guided Laser Ablation System (9736422)?

Visualase V2 MRI-guided Laser Ablation System (9736422) is manufactured by Medtronic Navigation.

What is the FDA product code for Visualase V2 MRI-guided Laser Ablation System (9736422)?

The FDA product code for Visualase V2 MRI-guided Laser Ablation System (9736422) is ONO.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.