Cleared Special

GREENLIGHT MOXY FIBER OPTIC

K120870 · American Medical Systems · General & Plastic Surgery

Jun 2012

Decision

85d

Days

Class 2

Risk

About This 510(k) Submission

K120870 is an FDA 510(k) clearance for the GREENLIGHT MOXY FIBER OPTIC, a Powered Laser Surgical Instrument (Class II — Special Controls, product code GEX), submitted by American Medical Systems (San Jose, US). The FDA issued a Cleared decision on June 15, 2012, 85 days after receiving the submission on March 22, 2012. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4810.

Submission Details

510(k) Number	K120870 FDA.gov
FDA Decision	Cleared SESE
Date Received	March 22, 2012
Decision Date	June 15, 2012
Days to Decision	85 days
Submission Type	Special
Review Panel	General & Plastic Surgery (SU)
Summary	Summary PDF

Device Classification

Product Code	GEX — Powered Laser Surgical Instrument
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 878.4810
Definition	A Laser (light Amplification By Stimulated Emission Of Radiation) Based Device Having Coherence, Collimated And Typically Monochromatic Radiation. Typically Indicated To To Cut, Destroy, Remove Or Coagulate Tissue, Generally Soft Tissue, For General Surgical Purpose In Medical Specialties Of General And Plastic Surgery, Dermatology/aesthetic, Podiatry, Otolaryngology (ent), Gynecology, Neurosurgery, Orthopedics (soft Tissue), Dental And Oral Surgery, And Dentistry. The Classification Regulation 21 Cfr 878.4810 Describes A Device That Is Carbon Dioxide Or Argon Laser Intended To Cut, Destroy, Remove Or Coagulate Tissue By The Light.