Pectus System Pt-2544
Pectus System Pt-2544 is a Class II device made by Biomet Microfixation, Inc, cleared under FDA 510(k) K061384 on 6 Jun 2006 and listed in FDA GUDID since 22 May 2018 (UDI-DI 00841036249755), active as of 23 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 | Number00841036249755 | Date22 May 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK061384 | Date6 Jun 2006 | StatusActive |
Official records
- AccessGUDID record 00841036249755
- FDA 510(k) database K061384
Across registries
- FDA 510(k) K061384 decided 6 Jun 2006 Active
- FDA GUDID UDI-DI 00841036249755 listed 22 May 2018 Listed
Timeline
- Cleared FDA 510(k) K061384
- Listed FDA GUDID 00841036249755
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Pectus System
- Generic name
- Funnel chest remodelling bar
- Model / reference
- PT-2544
- Primary DI / UDI-DI
- 00841036249755
- 510(k) Number
- FDA product code
- HRS
- GMDN term
- Funnel chest remodelling bar
- Device class
- Class II
- Regulation number
- 888.3030
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization