Who is the manufacturer of INFINITI VISION SYSTEM EVERGREEN II AUTOSERT IOL INJECTOR HANDPIECE?

Alcon Manufacturing, Ltd. filed the 510(k) submission for INFINITI VISION SYSTEM EVERGREEN II AUTOSERT IOL INJECTOR HANDPIECE (K112425).

What is the FDA product code for INFINITI VISION SYSTEM EVERGREEN II AUTOSERT IOL INJECTOR HANDPIECE?

HQC. It is classified under 21 CFR 886.4670 as a Class 2 device in the Ophthalmic panel.

What is the regulatory pathway for INFINITI VISION SYSTEM EVERGREEN II AUTOSERT IOL INJECTOR HANDPIECE?

510(k) clearance (submission type: Traditional).

What are the predicate devices for INFINITI VISION SYSTEM EVERGREEN II AUTOSERT IOL INJECTOR HANDPIECE?

Infiniti® Vision System (K021566); Infiniti® Vision System with OZil® IP (K082845); Alcon UltraChopper Tip (K091777); AquaLase Capsule Wash Tip (K093210); Monarch III IOL Delivery System (K063155).

Who can help prepare an FDA 510(k) submission like INFINITI VISION SYSTEM EVERGREEN II AUTOSERT IOL INJECTOR HANDPIECE?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

INFINITI VISION SYSTEM EVERGREEN II AUTOSERT IOL INJECTOR HANDPIECE

K112425 · Alcon Manufacturing, Ltd. · HQC · Nov 21, 2011 · Ophthalmic

Device Facts

Record ID	K112425
Device Name	INFINITI VISION SYSTEM EVERGREEN II AUTOSERT IOL INJECTOR HANDPIECE
Applicant	Alcon Manufacturing, Ltd.
Product Code	HQC · Ophthalmic
Decision Date	Nov 21, 2011
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 886.4670
Device Class	Class 2
Attributes	Therapeutic

Intended Use

The Infinit® Vision System is indicated for emulsification, separation, and removal of cataracts, the removal of residual cortical material and lens epithelial cells, vitreous aspiration and cutting associated with anterior vitrectomy, bipolar coagulation, and intra-ocular lens injection. The AutoSert™ IOL Injector Handpiece is intended to deliver qualified AcrySof® intraocular lenses into the eye following cataract removal. The following system modalities additionally support the described indications: - Ultrasound with UltraChopper Tip achieves the functionality of cataract separation. - AquaLase achieves the functionality for removal of residual cortical material and lens epithelial cells - The AutoSert ™ IOL Injector Handpiece achieves the functionality of injection of intraocular lenses. The AutoSert™ is indicated for use with ACRYSOF lenses SN60WF and SN6AD1, as well as approved AcrySof lenses that are specifically indicated for use with this inserter, as indicated in the approved labeling of those lenses.

Device Story

Infiniti® Vision System is a modular phacofragmentation system for cataract surgery. It utilizes ultrasound (with UltraChopper tip), AquaLase technology, and the AutoSert™ IOL injector handpiece to emulsify, separate, and remove cataracts, aspirate vitreous, perform bipolar coagulation, and inject IOLs. Operated by surgeons in clinical settings, the system provides integrated control over surgical modalities. The 'Power Watch' feature monitors system performance. The device processes user inputs to manage fluidics and energy delivery for lens removal and IOL insertion. By automating key surgical steps, the system enhances surgical efficiency and precision, potentially improving patient outcomes during cataract extraction and lens replacement procedures.

Clinical Evidence

No clinical data provided. Substantial equivalence is supported by non-clinical bench testing, including biocompatibility (ISO 10993 series), sterilization validation (ISO 11135-1), and electrical safety/EMC testing (IEC 60601 series).

Technological Characteristics

Modular phacofragmentation system. Components include ultrasound handpieces, AquaLase, and AutoSert IOL injector. Materials comply with ISO 10993. Sterilization via EtO for single-use accessories; reusable handpieces are reprocessable. Complies with IEC 60601-1 (safety), IEC 60601-1-2 (EMC), and IEC 80601-2-58 (lens removal/vitrectomy).

Indications for Use

Indicated for patients undergoing cataract surgery requiring emulsification, separation, and removal of cataracts, cortical material, and lens epithelial cells; anterior vitrectomy; bipolar coagulation; and intraocular lens (IOL) implantation. AutoSert™ handpiece is indicated for delivery of specific AcrySof® IOLs.

Regulatory Classification

Identification

A phacofragmentation system is an AC-powered device with a fragmenting needle intended for use in cataract surgery to disrupt a cataract with ultrasound and extract the cataract.

Predicate Devices

Infiniti® Vision System (K021566)
Infiniti® Vision System with OZil® IP (K082845)
Alcon UltraChopper Tip (K091777)
AquaLase Capsule Wash Tip (K093210)
Monarch III IOL Delivery System (K063155)

Related Devices

K121555 — CENTURION VISION SYSTEM · Alcon Laboratories, Inc. · Dec 21, 2012
K120912 — INFINITI(R) VISION SYSTEM · Alcon Manufacturing, Ltd. · Jun 15, 2012
K082845 — INFINITI VISION SYSTEM WITH OZIL IP · Alcon Research, Ltd. · Feb 12, 2009
K021566 — INFINITI · Alcon Laboratories, Inc. · Jul 2, 2002
K141065 — CONSTELLATION VISION SYSTEM · Alcon Research, Ltd. · Aug 22, 2014

Submission Summary (Full Text)

{0}------------------------------------------------ NOV 2 1 2011 k112425 # PREMARKET NOTIFICATION 510(k) SUMMARY The submitter of the 510(k) is: Martin A. Kaufman Director. Regulatory Affairs Alcon Research, Ltd. 18500 Alton Parkway Irvine, CA 92618 Phone: (949) 753-6250 Fax: (949) 753-6237 Device Subject to this 510(k): Trade Name: Common Name: Classification Name: Infiniti® Vision System Phacofragmentation System Phacofragmentation System (per 21 CFR 886.4670) ## Predicate Devices: The legally marketed devices(s) to which we are claiming equivalence to are: | 510(k) Number | Device | |---------------|---------------------------------------| | K021566 | Infiniti® Vision System | | K082845 | Infiniti® Vision System with OZil® IP | | K091777 | Alcon UltraChopper Tip | | K093210 | AquaLase Capsule Wash Tip | | K063155 | Monarch III IOL Delivery System | #### Device Description The Infinit® Vision System is an enhanced version of the Infinit® Vision System with OZil® IP (K082845) that is modular in design and incorporates the Power Watch feature, along with the Alcon UltraChopper Tip, the AquaLase Capsule Wash Tip, the AutoSert™ IOL Injector, and its associated software. {1}------------------------------------------------ # Indications for Use: The Infinity Vision System is indicated for emulsification, separation, and removal of cataracts, the removal of residual cortical material and lens epithelial cells, vitreous aspiration and cutting associated with anterior vitrectomy, bipolar coagulation, and intraocular lens injection. The AutoSert™ IOL Injector Handpiece is intended to deliver qualified AcrySof® intraocular lenses into the eye following cataract removal. The following system modalities additionally support the described indications: - Ultrasound with UltraChopper Tip achieves the functionality of cataract separation. - - AquaLase achieves the functionality for removal of residual cortical material and lens epithelial cells - The AutoSert™ IOL Iniector Handpiece achieves the functionality of injection of । intraocular lenses. The AutoSert™ is indicated for use with ACRYSOF lenses SN60WF and SN6AD1, as well as approved Acrysof lenses that are specifically indicated for use with this inserter, as indicated in the approved labeling of those lenses. ## Brief Summary of Nonclinical test and Results: Safety tests of the Infinity Vision System have demonstrated its compliance with applicable requirements of the following standards: | Standard # | Title | |-------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | 11135-1:2007 ISO | Sterilization of health care products - Ethylene oxide - Requirements for development, validation, and routine control of a sterilization process for medical devices. | | 11979-3:2006 BS EN ISO | Ophthalmic implants - Intraocular Lenses - Part 3: Mechanical properties and test methods | | 14971:2007 EN ISO | Medical Devices: Application of Risk Management to Medical Devices | | IEC 60601-1: 1988, A1:1991, A2:1995 | Medical Electrical Equipment - Part 1: General requirements for safety | | IEC 60601-1-1: 2000 | Medical electrical equipment. Part 1-1: General requirement for safety - Collateral standard: Safety requirements for medical electrical systems | | EN 60601-1-2: 2004 | Medical electrical equipment - Part 1: General requirements for safety 2. Collateral Standard: Electromagnetic compatibility - Requirements and tests | | IEC 60601-1-4: 2000 | Medical electrical equipment - Part 1: General requirements for safety - 4. Collateral standard: Programmable electrical medical systems. | | IEC 60601-1-6: 2006 | Medical electrical equipment - Part 1-6: General requirements for safety - Collateral standard: Usability. | | IEC 60601-2-2: 2006 | Medical electrical equipment - Part 2: Particular requirements for the safety of high frequency surgical equipment. | | IEC 80601-2-58: 2008 | Medical electrical equipment -- Part 2-58: Particular requirements for basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery | {2}------------------------------------------------ Biocompatibility evaluations of materials coming in contact with the patient fluid path have been performed to the following standards: | Standard # | Title | |-------------------------------|-----------------------------------------------------------------------------------------------------------------| | ISO 10993-1: 2009 | Biological Evaluation of Medical Devices -- Part 1: Evaluation and Testing within a Risk management Process | | ISO 10993-5: 2009 | Biological Evaluation of medical devices -- Part 5: Tests for In Vitro cytotoxicity | | ISO 10993-10: 2002/A1:2006 | Biological Evaluation of Medical Devices -- Part 10: Tests for irritation and delayed-type hypersensitivity | | ISO 10993-11: 2006 | Biological Evaluation of Medical Devices -- Part 11: Tests for systemic toxicity | | ISO 10993-12: 2007 | Biological Evaluation of Medical Devices --Part 12: Sample Preparation and Reference Materials | Many Infiniti® accessories are provided sterile and are intended for single use only. These products are EtO sterilized and the process has been validated per ISO 11135-1:2007: Medical Devices - Validation and Routine Control of Ethylene Oxide Sterilization. Reusable handpieces are provided non-sterile. Validated reprocessing instructions for cleaning, sterilization, and re-use of the handpieces are provided in the Directions for Use of the product. Technological characteristics affecting clinical performance are similar to that of predicate devices previously listed. The Infiniti® Vision System has been developed and will be manufactured in compliance with 21 CFR 820 and ISO 14971:2007. Non-clinical testing noted above has demonstrated that the functional requirements have been met and that the modified device is equivalent to the predicate device. #### Accessories Provided with the System (subject to change) | Configurations of tips and sleeves currently used with the Irrigation/Aspiration Handpiece. Description | |------------------------------------------------------------------------------------------------------------| | ASSY, SHIP, INTREPID POLYMER I/A TIP, STRAIGHT | | ASSY, SHIP, INTREPID POLYMER I/A TIP, ANGLED | | ASSY, SHIP, INTREPID POLYMER I/A TIP, CURVED | | I/A Tip 0.5 mm | | I/A Tip 0.2 mm | | I/A Tip 0.3 mm Small Bore | | I/A Tip 0.3 mm Small Bore Mod | | I/A Tip 0.3 mm Bent | | I/A Tip 0.3 mm Bent & Sand Blast | | I/A Tip .033 OD, .3mm, Intrepid | {3}------------------------------------------------ | Configurations of tips and sleeves currently used with the Irrigation/Aspiration Handpiece. | Description | |---------------------------------------------------------------------------------------------|-------------| | I/A Tip .033 OD, .3mm Bent, Intrepid | | | Silicone I/A Tip, Bent | | | Silicone I/A Tip, Straight | | | Ultraflow Tool/O-rings | | | Ultraflow IA Handpiece Comp | | | Ultraflow IA Handpiece Only | | | Ultraflow IA Tip STR | | | Ultraflow IA Tip CRVD | | | Ultraflow IA 45 | | | Ultraflow IA 90 | | | Ultraflow IA 120 | | | Ultraflow CNL STTL | | | Ultraflow Luer | | | Straight Tip, 3 mm | | | Ultraflow Tip Protector, Standalone | | | 45° Bent Tip, .3 mm | | | 90° Bent Tip, .3mm | | | Irrigation Only Luer | | | Curved Tip, .3mm | | | Threaded Tip - STTL | | | Ultraflow I/A Box | | | Replacement O-ring | | Configurations of Paks currently used with the Infiniti Vision System. | Description | |----------------------------------------------------------------------| | Ultrasound FMS, Basic | | Ultrasound FMS, Tipless, 0.9mm | | Ultrasound FMS, Tipless, 1.1mm | | Ultrasound FMS, Tipless, 0.9mm HIS | | Ultrasound FMS, Tipless, 1.1mm HIS | | Ultrasound FMS, 30° Round, 0.9 mm ABS | | Ultrasound FMS, 45° Round, 0.9 mm ABS | | Ultrasound FMS, 30° Kelman, 0.9 mm ABS | | Ultrasound FMS, 45° Kelman, 0.9 mm ABS | | Ultrasound FMS, 30° Round, 1.1 mm ABS | | Ultrasound FMS, 45° Round, 1.1 mm ABS | | Ultrasound FMS, 30° Kelman, 1.1 mm ABS | | Ultrasound FMS, 45° Kelman, 1.1 mm ABS | | Ultrasound FMS, 30° Round, 0.9 mm MicroTip Flared ABS | | Ultrasound FMS, 45° Round, 0.9 mm MicroTip Flared ABS | | Ultrasound FMS, 30° Kelman, 0.9 mm MicroTip Flared ABS | | Ultrasound FMS, 45° Kelman, 0.9 mm MicroTip Flared ABS | | Description | | Ultrasound FMS, 30° Round, 1.1 mm Flared ABS | | Ultrasound FMS, 45° Round, 1.1 mm Flared ABS | | Ultrasound FMS, 30° Kelman, 1.1 mm Flared ABS | | Ultrasound FMS, 45° Kelman, 1.1 mm Flared ABS | | Ultrasound FMS, 30° Round, 0.9 mm Mackool | | Ultrasound FMS, 45° Round, 0.9 mm Mackool | | Ultrasound FMS, 30° Kelman, 0.9 mm Mackool | | Ultrasound FMS, 45° Kelman, 0.9 mm Mackool | | Ultrasound FMS, 30° Round, 1.1 mm Mackool Flared ABS | | Ultrasound FMS, 45° Round, 1.1 mm Mackool Flared ABS | | Ultrasound FMS, 30° Kelman, 1.1 mm Mackool Flared ABS | | Ultrasound FMS, 45° Kelman, 1.1 mm Mackool Flared ABS | | Ultrasound FMS, 30° Round, 0.9 mm Tapered ABS | | Ultrasound FMS, 45° Round, 0.9 mm Tapered ABS | | Ultrasound FMS, 30° Kelman, 0.9 mm Tapered ABS | | Ultrasound FMS, 45° Kelman, 0.9 mm Tapered ABS | | Ultrasound FMS, Tipless, 0.9 Ultra | | Ultrasound FMS, 30° Kelman, 0.9 mm Mini Flared ABS, Ultra | | Ultrasound FMS, 45° Kelman, 0.9 mm Mini Flared ABS, Ultra | | Ultrasound FMS, 30° OZil 12, 0.9 mm Mini Flared ABS, Ultra | | Ultrasound FMS, 45° OZil 12, 0.9 mm Mini Flared ABS, Ultra | | Ultrasound FMS, 30° Kelman, 0.9 mm Mini Flared ABS | | Ultrasound FMS, 45° Kelman, 0.9 mm Mini Flared ABS | | Ultrasound FMS, 30° OZil 12, 0.9 mm Mini Flared ABS | | Ultrasound FMS, 45° OZil 12, 0.9 mm Mini Flared ABS | | Ultrasound FMS, Tipless, 0.9mm J | | Ultrasound FMS, Tipless, 1.1mm J | | Ultrasound FMS, Tipless, 0.9mm HIS J | | Ultrasound FMS, Tipless, 1.1mm HIS J | | Ultrasound FMS, Tipless, 0.9 Ultra J | | Ultrasound FMS, Intrepid, Basic | | Ultrasound FMS, Intrepid, Tipless, 0.9 Ultra | | Ultrasound FMS, Intrepid, Tipless, 1.1 Ultra | | Ultrasound FMS, Intrepid, Tipless, 0.9 Nano | | Ultrasound FMS, Intrepid, Tipless, 1.1 Nano | | Ultrasound FMS, Intrepid, 30° Kelman, 0.9 mm Mini-Flared ABS, Ultra | | Ultrasound FMS, Intrepid, 45° Kelman, 0.9 mm Mini-Flared ABS, Ultra | | Ultrasound FMS, Intrepid, Tipless, 0.9 | | Ultrasound FMS, Intrepid, 30° Kelman, 0.9 mm Mini Flared ABS, Nano | | Ultrasound FMS, Intrepid, 45° Kelman, 0.9 mm Mini Flared ABS, Nano | | Ultrasound FMS, Intrepid, 30° OZil 12, 0.9 mm Mini Flared ABS, Nano | | Ultrasound FMS, Intrepid, 45° OZil 12, 0.9 mm Mini Flared ABS, Nano | | Ultrasound FMS, Intrepid, 30° OZil 12, 0.9 mm Mini Flared ABS, Ultra | | Description | | Ultrasound FMS, Intrepid, 45° OZil 12, 0.9 mm Mini Flared ABS, Ultra | | Ultrasound FMS, Intrepid, 30° Kelman, 0.9 mm Mini Flared ABS, 0.9 | | Ultrasound FMS, Intrepid, 45° Kelman, 0.9 mm Mini Flared ABS, 0.9 | | Ultrasound FMS, Intrepid, 30° OZil 12, 0.9 mm Mini Flared ABS, 0.9 | | Ultrasound FMS, Intrepid, 45° OZil 12, 0.9 mm Mini Flared ABS, 0.9 | | Ultrasound FMS, Intrepid, Basic, J | | Ultrasound FMS, Intrepid, Tipless, 0.9 Ultra, J | | Ultrasound FMS, Intrepid, Tipless, 1.1 Ultra, J | | Ultrasound FMS, Intrepid, Tipless, 0.9 Nano, J | | Ultrasound FMS, Intrepid, Tipless, 1.1 Nano, J | | Ultrasound FMS, Intrepid, Tipless, 0.9 J | | INFI, Multipak, Basic Pak | | INFI, Multipak, 0.9mm Tipless | | INFI, Multipak, 1.1mm Tipless | | INFI MP Procedural Pouch Basic | | INFI MP Procedural Pouch 0.9mm | | INFI MP Procedural Pouch 1.1mm | | Infiniti MP Drain Bags | | INFI Multi-Pak Basic Stand Alone | | INFI Multi-Pak 0.9 Tipless Stand Alone | | INFI Multi-Pak 1.1 Tipless Stand Alone | | Ultrasound FMS, Intrepid Plus, Basic | | Ultrasound FMS, Intrepid Plus, 0.9 MM Tipless Ultra | | Ultrasound FMS, Intrepid Plus, 1.1 MM Tipless Ultra | | Ultrasound FMS, Intrepid Plus, 0.9 MM Tipless Nano | | Ultrasound FMS, Intrepid Plus, 1.1 MM Tipless Nano | | Ultrasound FMS, Intrepid Plus, 0.9 MM Mini-Flared ABS 30K, Ultra | | Ultrasound FMS, Intrepid Plus, 0.9 MM Mini-Flared ABS 45K, Ultra | | Ultrasound FMS, Intrepid Plus, 0.9 MM Tipless | | Ultrasound FMS, Intrepid Plus, 0.9 MM Mini-Flared ABS 30K, Nano | | Ultrasound FMS, Intrepid Plus, 0.9 MM Mini-Flared ABS 45K, Nano | | Ultrasound FMS, Intrepid Plus, 0.9 MM Mini-Flared ABS 30 OZil, Nano | | Ultrasound FMS, Intrepid Plus, 0.9 MM Mini-Flared ABS 45 OZil, Nano | | Ultrasound FMS, Intrepid Plus, 0.9 MM Mini-Flared ABS 30 OZil, Ultra | | Ultrasound FMS, Intrepid Plus, 0.9 MM Mini-Flared ABS 45 OZil, Ultra | | Ultrasound FMS, Intrepid Plus, 0.9 MM Mini-Flared ABS 30K | | Ultrasound FMS, Intrepid Plus, 0.9 MM Mini-Flared ABS 45K | | Ultrasound FMS, Intrepid Plus, 0.9 MM Mini-Flared ABS 30 OZil | | Ultrasound FMS, Intrepid Plus, 0.9 MM Mini-Flared ABS 45 OZil | {4}------------------------------------------------ · {5}------------------------------------------------ {6}------------------------------------------------ Image /page/6/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized caduceus, which is a symbol often associated with medicine and healthcare. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" are arranged in a circular pattern around the caduceus. Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002 NOV 2 1 2011 Alcon Research, Ltd. c/o Mr. Martin Kaufman, RAC Director, Regulatory Affairs 15800 Alton Parkway Irvine, CA 92816 Re: K112425 Trade/Device Name: Infiniti Vision System (Evergreen II) Regulation Number: 21 CFR 886.4670 Regulation Name: Phacofragmentation system Regulatory Class: II Product Codes: HQC, HQR, MLZ, KYB Dated: August 19, 2011 Received: August 23, 2011 Dear Mr. Kaufman: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 {7}------------------------------------------------ CFR Part 807): labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled. "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance. You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Sincerely yours. Kesia Alexander Malvina B. Evdelman, M.D. Director Division of Ophthalmic, Neurological, and Ear. Nose and Throat Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {8}------------------------------------------------ # INDICATIONS FOR USE STATEMENT 510(k) Number (if known): _ k1/2 425 Device Name: Infiniti® Vision System Indications for Use: The Infinit® Vision System is indicated for emulsification, separation, and removal of cataracts, the removal of residual cortical material and lens epithelial cells, vitreous aspiration and cutting associated with anterior vitrectomy, bipolar coagulation, and intra-ocular lens injection. The AutoSert™ IOL Injector Handpiece is intended to deliver qualified AcrySof® intraocular lenses into the eye following cataract removal. The following system modalities additionally support the described indications: - Ultrasound with UltraChopper Tip achieves the functionality of cataract separation. - AquaLase achieves the functionality for removal of residual cortical material and lens epithelial cells - The AutoSert ™ IOL Injector Handpiece achieves the functionality of injection of intraocular lenses. The AutoSert™ is indicated for use with ACRYSOF lenses SN60WF and SN6AD1, as well as approved AcrySof lenses that are specifically indicated for use with this inserter, as indicated in the approved labeling of those lenses. Prescription Use × AND/OR (Part 21 CFR 801 Subpart D) Over-The-Counter Use (21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) R (Division Sign-Off) Division of Ophthalmic, Neurological and Ear. Nose and Throat Devices 510(k) Number f/12425