Clearance Summary
HyperVit Vitrectomy Probe, 23 GA, HyperVit Vitrectomy Probe, 25+, HyperVit Vitrectomy Probe, 27+ received FDA 510(k) clearance under submission number K170520, sponsored by Alcon Research, Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2017-03-22.
- Submission: K170520
- Applicant / Sponsor: Alcon Research, Ltd.
- Clearance pathway: Special
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.4150
- Decision date: 2017-03-22
Classification & Regulation
This clearance is catalogued under FDA product code MLZ and 21 CFR 886.4150, within the Ophthalmic review panel as a Class II device.