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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name holder, head, neurosurgical (skull clamp)
510(k) Number K122225
Model 18911
Device Name STERILE RADIOLUCENT SKULL PINS
Original Applicant
BRAINLAB AG
kapellenstrasse 12
feldkirchen,  GM 85622
Original Contact alexander schwiersch
Regulation Number882.4460
Classification Product Code
HBL  
Date Received07/25/2012
Decision Date 04/26/2013
Decision substantially equivalent (SE)
Classification Advisory Committee Neurology
Review Advisory Committee Neurology
summary summary
Type Traditional
Reviewed by Third Party No
Expedited Review No
Combination Product No
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