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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 K023187
Device Name KSEA SPINOSCOPE
Applicant
Karl Storz Endoscopy
600 Corporate Pointe
Culver City,  CA  90230 -7600
Applicant Contact JAMES A LEE
Correspondent
Karl Storz Endoscopy
600 Corporate Pointe
Culver City,  CA  90230 -7600
Correspondent Contact JAMES A LEE
Regulation Number888.1100
Classification Product Code
HRX  
Date Received09/24/2002
Decision Date 12/02/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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