NERVE MONITORING CABLE— 510(k) K073229

Name: FDA 510(k) clearance K073229
Creator: U.S. Food and Drug Administration
Published: 2008-06-06

Substantially Equivalent

Pioneer Surgical Technology

FDA 510(k) clearance K073229 for NERVE MONITORING CABLE, Substantially Equivalent on 2008-06-06. Applicant: Pioneer Surgical Technology. Device class: 2.

Clearance details

Applicant: Pioneer Surgical Technology
Product code: Code GXZ
Device class: Class 2
Regulation: 21 CFR 882.1350
Advisory panel: Neurology
Date received: 2007-11-15
Decision date: 2008-06-06
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Marquette, MI, US

Download summary PDF View on FDA.gov ↗

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