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.
Approval for the manufacturing changes that were implemented as a result of the voluntary recall.
Device | MEMORY LENS ULTRAVIOLET-ABSORBING HYDROPHILIC POSTERIOR CHAMBER IOL |
Classification Name | Intraocular Lens |
Generic Name | Intraocular Lens |
Applicant | IOLTECH, S.A. |
Date Received | 2000-07-17 |
Decision Date | 2000-08-25 |
PMA | P960036 |
Supplement | S002 |
Product Code | HQL |
Advisory Committee | Ophthalmic |
Supplement Type | Normal 180 Day Track |
Expedited Review | No |
Combination Product | No |
Applicant Address | IOLTECH, S.A. 64 Schoosett Street penbroke, MA 02359-1882 |
Supplement Number | Date | Supplement Type |
---|---|---|
P960036 | Original Filing | |
S007 | 2002-07-08 | 30-day Notice |
S006 | 2002-06-06 | Real-time Process |
S005 | 2001-12-21 | Normal 180 Day Track |
S004 | 2000-09-18 | Normal 180 Day Track |
S003 | 2000-08-31 | Normal 180 Day Track |
S002 | 2000-07-17 | Normal 180 Day Track |
S001 | 1999-08-23 | Real-time Process |