510(k) K032751
K032751 is an FDA 510(k) premarket notification submitted by Advanced Neuromodulation Systems for the device "MODIFICATION TO RENEW LEAD EXTENSION". The FDA issued a decision of Substantially Equivalent on October 6, 2003. The device falls under product code GZB (Stimulator, Spinal-Cord, Implanted (Pain Relief)), a Class II device regulated under 21 CFR 882.5880. Advanced Neuromodulation Systems has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 6, 2003
- Date Received
- September 5, 2003
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Spinal-Cord, Implanted (Pain Relief)
- Device Class
- Class II
- Regulation Number
- 882.5880
- Review Panel
- NE
- Submission Type