Quantum M50 SC241
by IN2BONES
Quantum M50 SC241 is a Class II device made by IN2BONES, cleared under FDA 510(k) K191380 on 29 Jan 2020 and listed in FDA GUDID since 24 Jul 2020 (UDI-DI 03701337602680), active as of 22 Oct 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 | Number03701337602680 | Date24 Jul 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK191380 | Date29 Jan 2020 | StatusActive |
Official records
- AccessGUDID record 03701337602680
- FDA 510(k) database K191380
Across registries
- FDA 510(k) K191380 decided 29 Jan 2020 Active
- FDA GUDID UDI-DI 03701337602680 listed 24 Jul 2020 Listed
Timeline
- Cleared FDA 510(k) K191380
- Listed FDA GUDID 03701337602680
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Quantum
- Generic name
- Fixed-bearing total ankle prosthesis
- Model / Ref / Catalog
- M50 SC241
- Primary DI / UDI-DI
- 03701337602680
- 510(k) Number
- FDA product code
- HSN
- GMDN term
- Fixed-bearing total ankle prosthesis
- Device class
- Class II
- Regulation number
- 888.3110
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 31.40 MillimeterLength — 26.72 Millimeter