Cleared Traditional

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

K173346 · Lensar, Inc. · Ophthalmic

Mar 2018

Decision

128d

Days

Class 2

Risk

About This 510(k) Submission

K173346 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 March 2, 2018, 128 days after receiving the submission on October 25, 2017. This device falls under the Ophthalmic review panel. Regulated under 21 CFR 886.4390.

Submission Details

510(k) Number	K173346 FDA.gov
FDA Decision	Cleared SESE
Date Received	October 25, 2017
Decision Date	March 02, 2018
Days to Decision	128 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.