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FDA 510(k) Application Details - K173572
Device Classification Name
Filler, Bone Void, Calcium Compound
More FDA Info for this Device
510(K) Number
K173572
Device Name
Filler, Bone Void, Calcium Compound
Applicant
Kensey Nash Corporation dba DSM Biomedical
735 Pennsylvania Drive
Exton, PA 19431 US
Other 510(k) Applications for this Company
Contact
Susan Pileggi
Other 510(k) Applications for this Contact
Regulation Number
888.3045
More FDA Info for this Regulation Number
Classification Product Code
MQV
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/20/2017
Decision Date
05/09/2018
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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