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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 K862778
Device Name HALL CANNLULA SYSTEM
Applicant
Hall Surgical, Division of Zimmer, Inc.
P.O. Box 899
`Anta Barbara,  CA  93102
Applicant Contact DAVID D WELLINGTON
Correspondent
Hall Surgical, Division of Zimmer, Inc.
P.O. Box 899
`Anta Barbara,  CA  93102
Correspondent Contact DAVID D WELLINGTON
Regulation Number888.1100
Classification Product Code
HRX  
Date Received07/22/1986
Decision Date 09/08/1986
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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