510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K974708Substantially Equivalent

Gemini Standard and Mini Valves

Neurocare Group, Pleasant Prairie WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K974708 is the FDA 510(k) clearance record for GEMINI STANDARD AND MINI VALVES, a class II device, cleared for Neurocare Group on under FDA product code JXG (Shunt, Central Nervous System And Components). FDA records list one 510(k) clearance for Neurocare Group. As of , FDA records show no recalls naming K974708.

Clearance record

Decision date
Received
(83 days to decision)
Product code
JXG Shunt, Central Nervous System And Components
Regulation
21 CFR 882.5550
Device class
Class II
Review panel
Neurology
Applicant
Neurocare Group 8401 102nd St., Suite 200, Pleasant Prairie WI
510(k) summary
Summary
Third party review
No

Clearances, product code JXG

Trailing 12 months
5 clearances under product code JXG in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code JXG, trailing twelve months
MonthClearances
November 20252
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20261