RecallHawk

Visualase MRI-Guided Laser Ablation System (SW 3.4)

Medtronic Navigation, Inc.

Summary

Medtronic Navigation, Inc. received 510(k) clearance for Visualase MRI-Guided Laser Ablation System (SW 3.4), a ONO device. Cleared on 2022-01-07.

Details

Source

510(k) Clearance

External ID

K211269

Action Date

2022-01-07

Status

Traditional

Category

device

Product Code

ONO

Product Description

Visualase MRI-Guided Laser Ablation System (SW 3.4). Product code: ONO.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Medtronic Navigation, Inc. has received 10 total clearances in our database.

Medtronic Navigation, Inc. has 23 FDA actions in our database, including 13 recalls and 10 clearances.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Medtronic Navigation, Inc. have FDA actions?

Medtronic Navigation, Inc. has 23 FDA actions in our database, including 13 recalls and 10 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K211269" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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