Clearance Summary
PuraStat received FDA 510(k) clearance under submission number K253924, sponsored by 3-D Matrix Europe SAS. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2026-01-07.
- Submission: K253924
- Applicant / Sponsor: 3-D Matrix Europe SAS
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4456
- Decision date: 2026-01-07
Classification & Regulation
This clearance is catalogued under FDA product code QAU and 21 CFR 878.4456, within the General, Plastic Surgery review panel as a Class II device.