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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 Interlaminal
510(k) Number K050830
Device Name ZODIAC SPINAL FIXATION SYSTEM
Applicant
Alphatec/Nexmed
6110 Corte Del Cedro
Carlsbad,  CA  92009
Applicant Contact ELLEN A YARNALL
Correspondent
Alphatec/Nexmed
6110 Corte Del Cedro
Carlsbad,  CA  92009
Correspondent Contact ELLEN A YARNALL
Regulation Number888.3050
Classification Product Code
KWP  
Subsequent Product Codes
KWQ   MNH   MNI  
Date Received04/01/2005
Decision Date 06/22/2005
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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