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FDA 510(k) Application Details - K030682
Device Classification Name
Bone Grafting Material, Synthetic
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510(K) Number
K030682
Device Name
Bone Grafting Material, Synthetic
Applicant
BIOFORM, INC.
4133 COURTNEY ROAD, #10
FRANKSVILLE, WI 53126 US
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Contact
WILLIAM G HUBBARD
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Regulation Number
872.3930
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Classification Product Code
LYC
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More FDA Info for this Product Code
Date Received
03/05/2003
Decision Date
06/27/2003
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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