SlimTip™ MN10450-50A
by Advanced Neuromodulation Systems
SlimTip™ MN10450-50A is a Class III device made by Advanced Neuromodulation Systems, approved under FDA PMA P150004 on 11 Feb 2016 and listed in FDA GUDID since 21 Jul 2017 (UDI-DI 05415067027153), active as of 23 Oct 2026.
Active
PMA
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number05415067027153 | Date21 Jul 2017 | StatusListed |
| United States | FDA PMAAPPR | NumberP150004 | Date11 Feb 2016 | StatusActive |
Official records
- AccessGUDID record 05415067027153
- FDA PMA database P150004
Across registries
- FDA PMA P150004 decided 11 Feb 2016 Active
- FDA GUDID UDI-DI 05415067027153 listed 21 Jul 2017 Listed
Timeline
- Approved FDA PMA P150004
- Listed FDA GUDID 05415067027153
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA PMA Active
Specification
- Trade name
- SlimTip™
- Generic name
- Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection
- Model / Ref / Catalog
- MN10450-50A
- Primary DI / UDI-DI
- 05415067027153
- PMA number
- FDA product code
- PMP
- GMDN term
- Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection
- Device class
- Class III
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Size
- Length — 50.0000 Centimeter