Clearance Summary
Matreneu Percutaneous Balloon Compression Kit received FDA 510(k) clearance under submission number K220920, sponsored by Shenzhen Shineyard Medical Device Co. , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2022-09-07.
- Submission: K220920
- Applicant / Sponsor: Shenzhen Shineyard Medical Device Co. , Ltd.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class I
- Regulation citation: 21 CFR 882.4535
- Decision date: 2022-09-07
Classification & Regulation
This clearance is catalogued under FDA product code HAO and 21 CFR 882.4535, within the Neurology review panel as a Class I device.