510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K211269Substantially Equivalent

Visualase MRI-Guided Laser Ablation System (SW 3.4)

Medtronic Navigation, Inc, Louisville CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K211269 is the FDA 510(k) clearance record for Visualase MRI-Guided Laser Ablation System (SW 3.4), a class II device, cleared for Medtronic Navigation, Inc. on under FDA product code ONO (Neurosurgical Laser With Mr Thermography). FDA's definition for product code ONO reads: "Laser device for use to necrotize or coagulate soft tissue through interstitial irradition or thermal therapy under mri guidance and real time mr thermography in neurosurgery". FDA records list 85 510(k) clearances for Medtronic Navigation, Inc., from to . As of , FDA records show one recall naming K211269.

Clearance record

Decision date
Received
(255 days to decision)
Product code
ONO Neurosurgical Laser With Mr Thermography
Regulation
21 CFR 878.4810
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Medtronic Navigation, Inc. 826 Coal Creek Cir., Louisville CO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code ONO

Trailing 12 months
3 clearances under product code ONO in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code ONO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20261
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260