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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Surgical With Orthopedic Accessories, Ac-Powered
510(k) Number K881060
Device Name OSI RIZZOLI TRAUMA TABLE (ELECTRIC VERSION)
Applicant
ORTHOPEDIC SYSTEMS, INC.
1897 NATIONAL AVE.
HAYWARD,  CA  94545
Applicant Contact ROBERT R MOORE
Correspondent
ORTHOPEDIC SYSTEMS, INC.
1897 NATIONAL AVE.
HAYWARD,  CA  94545
Correspondent Contact ROBERT R MOORE
Regulation Number878.4960
Classification Product Code
JEA  
Date Received03/04/1988
Decision Date 03/25/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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