510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K094054Substantially Equivalent

Modifcation to: Nuvasive Neurovision EMG Endotracheal Tube

NuVasive Inc, San Diego CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K094054 is the FDA 510(k) clearance record for MODIFCATION TO: NUVASIVE NEUROVISION EMG ENDOTRACHEAL TUBE, a class II device, cleared for Nuvasive, Inc. on under FDA product code GWF (Stimulator, Electrical, Evoked Response). FDA records list 92 510(k) clearances for Nuvasive, Inc., from to . As of , FDA records show no recalls naming K094054.

Clearance record

Decision date
Received
(134 days to decision)
Product code
GWF Stimulator, Electrical, Evoked Response
Regulation
21 CFR 882.1870
Device class
Class II
Review panel
Neurology
Applicant
Nuvasive, Inc. 4545 Towne Centre Ct., San Diego CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GWF

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