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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Rongeur, Powered
510(k) Number K062413
Device Name AESCULAP PNEUMATIC KERRISON
Applicant
AESCULAP, INC.
3773 Corporate Parkway
Center Valley,  PA  18034
Applicant Contact KATHY A RACOSKY
Correspondent
AESCULAP, INC.
3773 Corporate Parkway
Center Valley,  PA  18034
Correspondent Contact KATHY A RACOSKY
Regulation Number882.4845
Classification Product Code
HAD  
Date Received08/17/2006
Decision Date 11/21/2006
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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