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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Laparoscope, General & Plastic Surgery
510(k) Number K930224
Device Name STRYKER ARTHROSCOPIC ACCESSORIES
Applicant
Stryker Corp.
210 Baypointe Pkwy.
San Jose,  CA  95134
Applicant Contact SHAUN GOLDEN
Correspondent
Stryker Corp.
210 Baypointe Pkwy.
San Jose,  CA  95134
Correspondent Contact SHAUN GOLDEN
Regulation Number876.1500
Classification Product Code
GCJ  
Date Received01/15/1993
Decision Date 06/30/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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