510(k) K221823

Cionic Neural Sleeve NS-100 by Cionic — Product Code GZI

K221823 is an FDA 510(k) premarket notification submitted by Cionic for the device "Cionic Neural Sleeve NS-100". The FDA issued a decision of Substantially Equivalent on July 21, 2022. The device falls under product code GZI (Stimulator, Neuromuscular, External Functional), a Class II device regulated under 21 CFR 882.5810. Cionic has at least 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 21, 2022
Date Received
June 23, 2022
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stimulator, Neuromuscular, External Functional
Device Class
Class II
Regulation Number
882.5810
Review Panel
NE
Submission Type