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FDA 510(k) Application Details - K153323
Device Classification Name
Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
More FDA Info for this Device
510(K) Number
K153323
Device Name
Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
Applicant
SPINEOLOGY, INC.
7800 3RD STREET NORTH
SAINT PAUL, MN 55128-5455 US
Other 510(k) Applications for this Company
Contact
JACQUELINE A HAUGE
Other 510(k) Applications for this Contact
Regulation Number
888.3070
More FDA Info for this Regulation Number
Classification Product Code
NKB
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/18/2015
Decision Date
02/23/2016
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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