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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Appliance, Fixation, Spinal Intervertebral Body
510(k) Number K782061
Device Name SPINAL SURGERY INSTRUMENTATION
Applicant
Stuart Drug & Surgical Supply, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Stuart Drug & Surgical Supply, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number888.3060
Classification Product Code
KWQ  
Date Received12/11/1978
Decision Date 03/21/1979
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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