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FDA 510(k) Application Details - K161173
Device Classification Name
More FDA Info for this Device
510(K) Number
K161173
Device Name
Avenue« T TLIF Cage
Applicant
LDR SPINE USA, INC.
13785 RESEARCH BLVD, SUITE 200
AUSTIN, TX 78750 US
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Contact
JOHN ROSSMAN
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Regulation Number
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Classification Product Code
OVD
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Date Received
04/26/2016
Decision Date
09/28/2016
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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