510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K112469Substantially Equivalent

General Prupose Localizers and Adapters-New Accessories for Sonowand System

Sonowand AS, Fridley MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K112469 is the FDA 510(k) clearance record for GENERAL PRUPOSE LOCALIZERS AND ADAPTERS-NEW ACCESSORIES FOR SONOWAND SYSTEM, a class II device, cleared for Sonowand AS on under FDA product code HAW (Neurological Stereotaxic Instrument). FDA records list 2 510(k) clearances for Sonowand AS, from to . As of , FDA records show no recalls naming K112469.

Clearance record

Decision date
Received
(210 days to decision)
Product code
HAW Neurological Stereotaxic Instrument
Regulation
21 CFR 882.4560
Device class
Class II
Review panel
Neurology
Applicant
Sonowand AS 435 Rice Creek Terrance NE, Fridley MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HAW

Trailing 12 months
4 clearances under product code HAW 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 HAW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20261
June 20260
July 20260
August 20261
September 20261
October 20260