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FDA 510(k) Application Details - K992239
Device Classification Name
Prosthesis, Chin, Internal
More FDA Info for this Device
510(K) Number
K992239
Device Name
Prosthesis, Chin, Internal
Applicant
PILLAR SURGICAL, INC.
P.O. BOX 8141
LA JOLLA, CA 92038 US
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Contact
ROB FRITZENKOTTER
Other 510(k) Applications for this Contact
Regulation Number
878.3550
More FDA Info for this Regulation Number
Classification Product Code
FWP
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More FDA Info for this Product Code
Date Received
07/02/1999
Decision Date
11/22/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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