PMT Platinum Depthalon Depth Electrode— 510(k) K151790

Name: FDA 510(k) clearance K151790
Creator: U.S. Food and Drug Administration
Published: 2016-07-14

Substantially Equivalent

Pmt Corporation

FDA 510(k) clearance K151790 for PMT Platinum Depthalon Depth Electrode, Substantially Equivalent on 2016-07-14. Applicant: Pmt Corporation. Device class: 2.

Clearance details

Applicant: Pmt Corporation
Product code: Code GZL
Device class: Class 2
Regulation: 21 CFR 882.1330
Advisory panel: Neurology
Date received: 2015-07-01
Decision date: 2016-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chanhassen, MN, US

Download summary PDF View on FDA.gov ↗

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