510(k) K110118

STIMTRODE SINGLE USE NERVE STIMULATOR by Xavant Technology (Pty), Ltd. — Product Code BXN

K110118 is an FDA 510(k) premarket notification submitted by Xavant Technology (Pty), Ltd. for the device "STIMTRODE SINGLE USE NERVE STIMULATOR". The FDA issued a decision of Substantially Equivalent on February 17, 2011. The device falls under product code BXN (Stimulator, Nerve, Battery-Powered), a Class II device regulated under 21 CFR 868.2775. Xavant Technology (Pty), Ltd. has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 17, 2011
Date Received
January 18, 2011
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stimulator, Nerve, Battery-Powered
Device Class
Class II
Regulation Number
868.2775
Review Panel
AN
Submission Type