510(k) K201873

Sparrow Therapy System by Spark Biomedical, Inc. — Product Code PZR

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 2, 2021
Date Received
July 7, 2020
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Percutaneous Nerve Stimulator For Opioid Withdrawal
Device Class
Class II
Regulation Number
882.5896
Review Panel
NE
Submission Type

Stimulate nerve branches to aid in the reduction of symptoms associated with substance use disorders.