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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Arthroscope
510(k) Number K841241
Device Name ANTERIOR CRUCIATE LIGAMENT GRASPER
Applicant
Surgical Products Corp.
P.O. Box 569
Salt Lake City,  UT  84110
Applicant Contact RICHARD W BAGGETT
Correspondent
Surgical Products Corp.
P.O. Box 569
Salt Lake City,  UT  84110
Correspondent Contact RICHARD W BAGGETT
Regulation Number888.1100
Classification Product Code
HRX  
Date Received03/23/1984
Decision Date 02/06/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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