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510(k) K920256

SPINE MOTION ANALYZER WITH EMG by Orthopedic Systems, Inc. — Product Code KQX

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 10, 1992
Date Received
January 21, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Goniometer, Ac-Powered
Device Class
Class I
Regulation Number
888.1500
Review Panel
NE
Submission Type

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