Wiggins Medical 52-141-008B
Wiggins Medical 52-141-008B is a Class II device made by Ebner Medical LLC, cleared under FDA 510(k) K200383 on 21 Jul 2020 and listed in FDA GUDID since 29 Mar 2021 (UDI-DI 00840217903301), active as of 2 Nov 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00840217903301 | Date29 Mar 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK200383 | Date21 Jul 2020 | StatusActive |
Official records
- AccessGUDID record 00840217903301
- FDA 510(k) database K200383
Across registries
- FDA 510(k) K200383 decided 21 Jul 2020 Active
- FDA GUDID UDI-DI 00840217903301 listed 29 Mar 2021 Listed
Timeline
- Cleared FDA 510(k) K200383
- Listed FDA GUDID 00840217903301
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Wiggins Medical
- Generic name
- Spinal rongeur
- Model / Ref / Catalog
- 52-141-008B
- Primary DI / UDI-DI
- 00840217903301
- 510(k) Number
- FDA product code
- HAE
- GMDN term
- Spinal rongeur
- Device class
- Class II
- Regulation number
- 882.4840
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 7 InchWidth — .8 Millimeter