510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K202072Substantially Equivalent

MindsEye Expandable Port

Minnetronix Neuro, Inc., St Paul MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K202072 is the FDA 510(k) clearance record for MindsEye Expandable Port, a class II device, cleared for Minnetronix Neuro, Inc. on under FDA product code GZT (Retractor, Self-Retaining, For Neurosurgery). FDA records list one 510(k) clearance for Minnetronix Neuro, Inc. As of , FDA records show no recalls naming K202072.

Clearance record

Decision date
Received
(30 days to decision)
Product code
GZT Retractor, Self-Retaining, For Neurosurgery
Regulation
21 CFR 882.4800
Device class
Class II
Review panel
Neurology
Applicant
Minnetronix Neuro, Inc. 1635 Energy Park Dr., St Paul MN
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code GZT

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