Cleared Special

K092023 - NAVIJECT SUB2-1P

K092023 is an FDA 510(k) clearance for NAVIJECT SUB2-1P, manufactured by Medicel AG. The device is a Class 1 Ophthalmic device with product code MSS cleared through the Special 510(k) pathway after a 22-day FDA review.

K092023 · Medicel AG · Ophthalmic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2009
Decision
22d
Days
Class 1
Risk

K092023 is an FDA 510(k) clearance for the NAVIJECT SUB2-1P, MODEL: LP604430. Classified as Folders And Injectors, Intraocular Lens (iol) (product code MSS), Class I - General Controls.

Submitted by Medicel AG (Hasbrouck Heights, US). The FDA issued a Cleared decision on July 28, 2009 after a review of 22 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4300 - the FDA ophthalmic device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Medicel AG devices

FDA 510(k) Submission Details - K092023

510(k) Number K092023 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 06, 2009
Decision Date July 28, 2009
Days to Decision 22 days
Submission Type Special
Review Panel Ophthalmic (OP)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
88d faster than avg
Panel avg: 110d · This submission: 22d
Pathway characteristics
Modification to existing cleared device.

MSS Device Classification - Class 1, General Controls

Product Code MSS Folders And Injectors, Intraocular Lens (iol)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.4300
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - MSS Folders And Injectors, Intraocular Lens (iol)

All 18
Devices cleared under the same product code (MSS) and FDA review panel - the closest regulatory comparables to K092023.
Crystalsert Lens Delivery System
K173480 · Bausch & Lomb, Inc. · Dec 2017
Bausch + Lomb Injector System
K151102 · Bausch & Lomb, Inc. · May 2015
BAUSCH & LOMB IOL INJECTOR
K113852 · Bausch & Lomb, Inc. · Sep 2012
EPIPHANY INJECTION SYSTEM
K090161 · Staar Surgical Co. · Jun 2009
CRYSTALSERT CRYSTALENS DELIVERY SYSTEM
K082944 · Bausch & Lomb, Inc. · Oct 2008
MPORT FOLDABLE LENS PLACEMENT SYSTEM
K970727 · Chiron Vision Corp. · Dec 1997