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FDA 510(k) Application Details - K202496
Device Classification Name
Plate, Fixation, Bone
More FDA Info for this Device
510(K) Number
K202496
Device Name
Plate, Fixation, Bone
Applicant
Globus Medical Inc.
2560 General Armistead Ave.
Audubon, PA 19403 US
Other 510(k) Applications for this Company
Contact
Jennifer Antonacci
Other 510(k) Applications for this Contact
Regulation Number
888.3030
More FDA Info for this Regulation Number
Classification Product Code
HRS
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/31/2020
Decision Date
10/29/2020
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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