LHG — Electrode, Spinal Epidural Class II
FDA product code LHG covers "Electrode, Spinal Epidural", a Class II medical device regulated under 21 CFR 882.5880. Submissions are reviewed by the Neurology panel. Devices under this code are implants. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- LHG
- Device Class
- Class II
- Regulation Number
- 882.5880
- Submission Type
- Review Panel
- NE
- Medical Specialty
- Neurology
- Implant
- Yes
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K110609 | st jude medical | EPIDUCER LEAD DELIVERY SYSTEM | June 24, 2011 |