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FDA 510(k) Application Details - K961976
Device Classification Name
Plate, Bone
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510(K) Number
K961976
Device Name
Plate, Bone
Applicant
BIOMEDICS
1920 N STREET, NW SUITE 650
WASHINGTON, DC 20036 US
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Contact
BRUCE F MACKLER
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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
05/20/1996
Decision Date
08/16/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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