510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K090455Substantially Equivalent

Provox Vega, Model 8130-8135

Atos Medical AB, Horby, SE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K090455 is the FDA 510(k) clearance record for PROVOX VEGA, MODEL 8130-8135, a class II device, cleared for Atos Medical AB on under FDA product code EWL (Prosthesis, Laryngeal (Taub)). FDA records list 15 510(k) clearances for Atos Medical AB, from to . As of , FDA records show no recalls naming K090455.

Clearance record

Decision date
Received
(102 days to decision)
Product code
EWL Prosthesis, Laryngeal (Taub)
Regulation
21 CFR 874.3730
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Atos Medical AB Kraftgatan 8, Horby, SE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code EWL

Trailing 12 months

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

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