AceConnex™ PSF141140-6
by Allosource
AceConnex™ PSF141140-6 is a Class II device made by Allosource, cleared under FDA 510(k) K213046 on 27 Jun 2023 and listed in FDA GUDID since 8 Nov 2023 (UDI-DI 00810053078709), 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 | Number00810053078709 | Date8 Nov 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK213046 | Date27 Jun 2023 | StatusActive |
Official records
- AccessGUDID record 00810053078709
- FDA 510(k) database K213046
Across registries
- FDA 510(k) K213046 decided 27 Jun 2023 Active
- FDA GUDID UDI-DI 00810053078709 listed 8 Nov 2023 Listed
Timeline
- Cleared FDA 510(k) K213046
- Listed FDA GUDID 00810053078709
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- AceConnex™
- Generic name
- Cadaveric-donor fascia allograft
- Model / Ref / Catalog
- PSF141140-6
- Primary DI / UDI-DI
- 00810053078709
- 510(k) Number
- FDA product code
- GAT
- GMDN term
- Cadaveric-donor fascia allograft
- Device class
- Class II
- Regulation number
- 878.5000
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 140 MillimeterOuter Diameter — 5.5 Millimeter
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