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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stimulator, Muscle, Powered, For Muscle Conditioning
510(k) Number K192940
Device Name CoolTone
Applicant
Zimmer Medizinsysteme GmbH
Junkerstrasse 9
Neu-Ulm,  DE 89231
Applicant Contact Ute Hauss
Correspondent
Quality and Regulatory Services
151 Glensondale Rd.
Stow,  MA  01775
Correspondent Contact Scott Blood
Regulation Number890.5850
Classification Product Code
NGX  
Date Received10/18/2019
Decision Date 11/15/2019
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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