VERTIS PNT CONTROL UNIT, MODEL CU 100; VERTIS PNT SAFEGUIDE-CERVICAL, MODEL SG 102-XXX— 510(k) K022241

Name: FDA 510(k) clearance K022241
Creator: U.S. Food and Drug Administration
Published: 2002-09-11

Substantially Equivalent

Vertis Neuroscience, Inc.

FDA 510(k) clearance K022241 for VERTIS PNT CONTROL UNIT, MODEL CU 100; VERTIS PNT SAFEGUIDE-CERVICAL, MODEL SG 102-XXX, Substantially Equivalent on 2002-09-11. Applicant: Vertis Neuroscience, Inc.. Device class: 2.

Clearance details

Applicant: Vertis Neuroscience, Inc.
Product code: Code NHI
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2002-07-11
Decision date: 2002-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

Download summary PDF View on FDA.gov ↗

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