Pectus System 01-3707-P
by Biomet Microfixation, Inc 2 variants
Pectus System 01-3707-P is a Class II device made by Biomet Microfixation, Inc, cleared under FDA 510(k) K972420 on 11 Aug 1997 and listed in FDA GUDID since 17 Jun 2020 (UDI-DI 00888233024990), 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 | Number00888233024990 | Date17 Jun 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK972420 | Date11 Aug 1997 | StatusActive |
Official records
- AccessGUDID record 00888233024990
- FDA 510(k) database K972420
Across registries
- FDA 510(k) K972420 decided 11 Aug 1997 Active
- FDA GUDID UDI-DI 00888233024990 listed 17 Jun 2020 Listed
Timeline
- Cleared FDA 510(k) K972420
- Listed FDA GUDID 00888233024990
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- Withdrawn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 / Ref / Catalog
- 01-3707-P
- Primary DI / UDI-DI
- 00888233024990
- 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