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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name instrument, surgical, non-powered
510(k) Number K863415
Device Name RAYLOR BONE IMPACTORS
Applicant
CEDAR SURGICAL, INC.
15265 MINNETONKA BLVD.
MINNETONKA,  MN  55345
Applicant Contact TERRY P CORBIN
Correspondent
CEDAR SURGICAL, INC.
15265 MINNETONKA BLVD.
MINNETONKA,  MN  55345
Correspondent Contact TERRY P CORBIN
Regulation Number882.4535
Classification Product Code
HAO  
Date Received09/03/1986
Decision Date 09/24/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
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