Clearance Summary
MODIFICATION TO LEKSELL STEREOTACTIC SYSTEM received FDA 510(k) clearance under submission number K031980, sponsored by Elekta Instrument AB. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2003-07-25.
- Submission: K031980
- Applicant / Sponsor: Elekta Instrument AB
- Clearance pathway: Special
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4560
- Decision date: 2003-07-25
Classification & Regulation
This clearance is catalogued under FDA product code HAW and 21 CFR 882.4560, within the Neurology review panel as a Class II device.