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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name spatula, orthopedic
510(k) Number K872281
Device Name RAYLOR FUSION FUNNEL
Applicant
CEDAR SURGICAL, INC.
15265 MINNETONKA BLVD.
MINNETONKA,  MN  55345
Applicant Contact QERRY P CORBIN
Correspondent
CEDAR SURGICAL, INC.
15265 MINNETONKA BLVD.
MINNETONKA,  MN  55345
Correspondent Contact QERRY P CORBIN
Regulation Number878.4800
Classification Product Code
HXR  
Date Received06/16/1987
Decision Date 11/02/1987
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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