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FDA 510(k) Application Details - K970256
Device Classification Name
Plate, Bone
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510(K) Number
K970256
Device Name
Plate, Bone
Applicant
MEDICON, E.G.
555 THIRTEENTH STREET, N.W.
WASHINGTON, DC 20004-1109 US
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Contact
HOWARD M HOLSTEIN, ESQ.
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Regulation Number
872.4760
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Classification Product Code
JEY
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More FDA Info for this Product Code
Date Received
01/23/1997
Decision Date
03/11/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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