Clearance Summary
TOPSLANE DMLC received FDA 510(k) clearance under submission number K060187, sponsored by Topslane International, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2006-07-27.
- Submission: K060187
- Applicant / Sponsor: Topslane International, LLC
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5710
- Decision date: 2006-07-27
Classification & Regulation
This clearance is catalogued under FDA product code IXI and 21 CFR 892.5710, within the Radiology review panel as a Class II device.