This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.
Change in the sterilization process parameters for the device.
| Device | TECNIS MULTIFOCAL SILICONE IOL/MODEL ZM900 & THE TECNIS MULTIFOCAL FOLDABLE ACRYLIC IOL MODEL ZMA00 |
| Classification Name | Lens, Multifocal Intraocular |
| Generic Name | Lens, Multifocal Intraocular |
| Applicant | Johnson & Johnson Surgical Vision, Inc. |
| Date Received | 2009-06-09 |
| Decision Date | 2009-07-17 |
| PMA | P080010 |
| Supplement | S003 |
| Product Code | MFK |
| Advisory Committee | Ophthalmic |
| Supplement Type | 30-day Notice |
| Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
| Expedited Review | No |
| Combination Product | No |
| Applicant Address | Johnson & Johnson Surgical Vision, Inc. 1700 E. St. Andrew Place santa Ana, CA 92705 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P080010 | Original Filing | |
| S021 | 2022-11-09 | 30-day Notice |
| S020 | 2020-12-10 | 30-day Notice |
| S019 | ||
| S018 | 2019-02-26 | 30-day Notice |
| S017 | 2018-12-21 | 30-day Notice |
| S016 | 2018-12-21 | 30-day Notice |
| S015 | 2018-04-11 | 30-day Notice |
| S014 | 2017-09-28 | 30-day Notice |
| S013 | 2016-06-01 | 30-day Notice |
| S012 | 2015-12-18 | 30-day Notice |
| S011 | 2015-06-26 | 30-day Notice |
| S010 | 2013-11-26 | 30-day Notice |
| S009 | 2013-05-24 | 30-day Notice |
| S008 | 2012-04-23 | 30-day Notice |
| S007 | 2012-01-30 | 30-day Notice |
| S006 | ||
| S005 | 2010-04-01 | 30-day Notice |
| S004 | 2009-06-30 | 30-day Notice |
| S003 | 2009-06-09 | 30-day Notice |
| S002 | 2009-04-28 | Normal 180 Day Track No User Fee |
| S001 | 2009-01-27 | Normal 180 Day Track |