Cleared Traditional

LENSAR Laser System - fs 3D (LLS-fs 3D)

K170576 · Lensar, Inc. · Ophthalmic

May 2017

Decision

67d

Days

Class 2

Risk

About This 510(k) Submission

K170576 is an FDA 510(k) clearance for the LENSAR Laser System - fs 3D (LLS-fs 3D), a Ophthalmic Femtosecond Laser (Class II — Special Controls, product code OOE), submitted by Lensar, Inc. (Orlando, US). The FDA issued a Cleared decision on May 5, 2017, 67 days after receiving the submission on February 27, 2017. This device falls under the Ophthalmic review panel. Regulated under 21 CFR 886.4390.

Submission Details

510(k) Number	K170576 FDA.gov
FDA Decision	Cleared SESE
Date Received	February 27, 2017
Decision Date	May 05, 2017
Days to Decision	67 days
Submission Type	Traditional
Review Panel	Ophthalmic (OP)
Summary	Summary PDF

Device Classification

Product Code	OOE — Ophthalmic Femtosecond Laser
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 886.4390
Definition	Precise Cutting Or Ablation Of Ocular Tissue, Indicated For The Anterior Capsulotomy During Cataract Surgery.