EXPEDIUM, VIPER. VIPER 2 SPINE SYSTEM— 510(k) K131802

Name: FDA 510(k) clearance K131802
Creator: U.S. Food and Drug Administration
Published: 2013-09-12

Substantially Equivalent

Depuy Spine, A Johnson & Johnson Company

FDA 510(k) clearance K131802 for EXPEDIUM, VIPER. VIPER 2 SPINE SYSTEM, Substantially Equivalent on 2013-09-12. Applicant: Depuy Spine, A Johnson & Johnson Company. Device class: 2.

Clearance details

Applicant: Depuy Spine, A Johnson & Johnson Company
Product code: Code OSH
Device class: Class 2
Regulation: 21 CFR 888.3070
Advisory panel: Orthopedic
Date received: 2013-06-19
Decision date: 2013-09-12
Decision: Substantially Equivalent
Clearance type: Special
Location: Raynham, MA, US

Download summary PDF View on FDA.gov ↗

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