Visualase V2 MRI-guided Laser Ablation System (9736422)
K-Number: K250307 · 2025-05-29
Device Summary
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. The listed applicant is Medtronic Navigation. The 510(k) number is K250307.
When did Visualase V2 MRI-guided Laser Ablation System (9736422) receive FDA 510(k) clearance?
Visualase V2 MRI-guided Laser Ablation System (9736422) received FDA 510(k) clearance on 2025-05-29, under 510(k) number K250307.
Who is the listed applicant for Visualase V2 MRI-guided Laser Ablation System (9736422)?
The FDA 510(k) record lists Medtronic Navigation as the applicant. This does not by itself establish the device manufacturer.
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.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Medtronic Navigation as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: ONO)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.