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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Operating-Room, Ac-Powered
510(k) Number K922371
Device Name SPINAL POSITIONING FRAME
Applicant
Rhino Mfg.
11321 Trade Center Dr., #260
Rancho Cordova,  CA  95742
Applicant Contact SHANE FISK
Correspondent
Rhino Mfg.
11321 Trade Center Dr., #260
Rancho Cordova,  CA  95742
Correspondent Contact SHANE FISK
Regulation Number878.4960
Classification Product Code
FQO  
Date Received05/20/1992
Decision Date 06/04/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
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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