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FDA 510(k) Application Details - K081540
Device Classification Name
Monitor, Spine Curvature
More FDA Info for this Device
510(K) Number
K081540
Device Name
Monitor, Spine Curvature
Applicant
PETER FISCHER
CHRISTOPHSTR. 2
TUBINGEN D72072 DE
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Contact
PETER FISCHER
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Regulation Number
000.0000
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Classification Product Code
LZW
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More FDA Info for this Product Code
Date Received
06/02/2008
Decision Date
02/20/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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