FDA 510(k) Application Details - K202505

Device Classification Name	Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease   More FDA Info for this Device
510(K) Number	K202505
Device Name	Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
Applicant	GetSet Surgical, SA Route de la Corniche 4 Epalinges 1066 CH Other 510(k) Applications for this Company
Contact	Ole Stoklund 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	08/31/2020
Decision Date	01/11/2021
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