MFX
- Product code
- MFX
- Device name
- Vessel Guard Or Cover, To Facilitate Revision Surgeries
- Device class
- Class 2
- 21 CFR
- 21 CFR 870.3470
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K)
- 510(k) clearances (all years, FDA)
- 2 (all years; only the last 3 years are listed here)
FDA classification definition
Wrap, patch, or cover intended to protect vessels from injury during surgery, with the secondary function of facilitating revision surgeries by providing a plane of dissection.
Official FDA classification page: MFX
Classification and pathway per current FDA publications. Data from openFDA (CC0).