AUDIT V AX 135— 510(k) K833298

Substantially Equivalent

Axonics, Inc.

FDA 510(k) clearance K833298 for AUDIT V AX 135, Substantially Equivalent on 1983-12-01. Applicant: Axonics, Inc.. Device class: 2.

Clearance details

Applicant
Axonics, Inc.
Product code
Code GWK
Device class
Class 2
Regulation
21 CFR 882.1845
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
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