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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name rod, fixation, intramedullary and accessories
510(k) Number K022225
Device Name VECTOR MEDICAL, INC., VECTOR TARGETING SYSTEM
Applicant
VECTOR MEDICAL, INC.
1886 LODGEPOLE DR.
MILTON,  FL  32583
Applicant Contact ERIN MCGURK
Correspondent
VECTOR MEDICAL, INC.
1886 LODGEPOLE DR.
MILTON,  FL  32583
Correspondent Contact ERIN MCGURK
Regulation Number888.3020
Classification Product Code
HSB  
Date Received07/10/2002
Decision Date 07/25/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Statement Statement
Type Special
Reviewed by Third Party No
Combination Product No
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