510(k) K963432

GUIDE WIRES FOR CANNULATED SCREWS by Orthopaedic Biosystems, Ltd. — Product Code LXT

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 13, 1996
Date Received
August 30, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
Device Class
Class II
Regulation Number
888.3030
Review Panel
OR
Submission Type