Clearance Summary
SKIN MESH DEVICE received FDA 510(k) clearance under submission number K861285, sponsored by Precision Modified Devices. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1986-04-17.
- Submission: K861285
- Applicant / Sponsor: Precision Modified Devices
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4820
- Decision date: 1986-04-17
Classification & Regulation
This clearance is catalogued under FDA product code GFD and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.