FDA 510(k) Application Details - K201926

Device Classification Name	Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease   More FDA Info for this Device
510(K) Number	K201926
Device Name	Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
Applicant	CarboFix Orthopedics Ltd. 11 HaÆhoshlim St. Herzeliya 4672411 IL Other 510(k) Applications for this Company
Contact	Hila Wachsler-Avrahami 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	07/10/2020
Decision Date	08/07/2020
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review