510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K110419Substantially Equivalent

Avs Aria Neuromonitoring Probe and Avs Aria Probe Dilators

Howmedica Osteonics Corp, Allendale NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K110419 is the FDA 510(k) clearance record for AVS ARIA NEUROMONITORING PROBE AND AVS ARIA PROBE DILATORS, a class II device, cleared for Stryker Spine on under FDA product code GXZ (Electrode, Needle). FDA records list 377 510(k) clearances for HOWMEDICA OSTEONICS CORP, from to . As of , FDA records show no recalls naming K110419.

Clearance record

Decision date
Received
(164 days to decision)
Product code
GXZ Electrode, Needle
Regulation
21 CFR 882.1350
Device class
Class II
Review panel
Neurology
Applicant
Stryker Spine 2 Pearl Ct., Allendale NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GXZ

Trailing 12 months

FDA records hold no clearances under product code GXZ in the trailing twelve months.

FDA records show no clearances under product code GXZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GXZ, 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 20260
October 20260