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FDA 510(k) Application Details - K222753
Device Classification Name
Orthopedic Stereotaxic Instrument
More FDA Info for this Device
510(K) Number
K222753
Device Name
Orthopedic Stereotaxic Instrument
Applicant
SeaSpine Orthopedics Corporation
5770 Armada Drive
Carlsband, CA 92008 US
Other 510(k) Applications for this Company
Contact
Laeitia Cousin
Other 510(k) Applications for this Contact
Regulation Number
882.4560
More FDA Info for this Regulation Number
Classification Product Code
OLO
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/12/2022
Decision Date
12/09/2022
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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