510(k) K110118
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