SPINE MOTION ANALYZER WITH EMG— 510(k) K920256

Name: FDA 510(k) clearance K920256
Creator: U.S. Food and Drug Administration
Published: 1992-08-10

Substantially Equivalent

Orthopedic Systems, Inc.

FDA 510(k) clearance K920256 for SPINE MOTION ANALYZER WITH EMG, Substantially Equivalent on 1992-08-10. Applicant: Orthopedic Systems, Inc.. Device class: 1.

Clearance details

Applicant: Orthopedic Systems, Inc.
Product code: Code KQX
Device class: Class 1
Regulation: 21 CFR 888.1500
Advisory panel: Orthopedic
Date received: 1992-01-21
Decision date: 1992-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hayward, CA, US

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