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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 K912871
Device Name INSIDE JOB
Applicant
3M HEALTH CARE, LTD.
3M CENTER, BLDG. 275-3E-08
P.O. BOX 33275
ST. PAUL,  MN  55133
Applicant Contact WILLARD D LARSON
Correspondent
3M HEALTH CARE, LTD.
3M CENTER, BLDG. 275-3E-08
P.O. BOX 33275
ST. PAUL,  MN  55133
Correspondent Contact WILLARD D LARSON
Regulation Number888.1100
Classification Product Code
HRX  
Date Received06/28/1991
Decision Date 08/09/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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