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FDA 510(k) Application Details - K955540
Device Classification Name
Manipulator, Plunger-Like Joint
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510(K) Number
K955540
Device Name
Manipulator, Plunger-Like Joint
Applicant
SPINALIGHT, INC.
320 A BELL PARK DR.
WOODSTOCK, GA 30188 US
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Contact
T. A. COX
Other 510(k) Applications for this Contact
Regulation Number
000.0000
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Classification Product Code
LXM
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/05/1995
Decision Date
03/04/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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