Atlas FDA

AcrySof IQ ReSTOR +3.0 D Multifocal Toric IOLs

FDA premarket approval P040020/S095 · decided 2020-08-28

Approval details

PMA number
P040020
Supplement
S095
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
AcrySof IQ ReSTOR +3.0 D Multifocal Toric IOLs
Generic name
Lens, multifocal intraocular
Applicant
Alcon Research, Ltd.
Date received
2020-07-31
Decision date
2020-08-28
Days to decision
28 days
Decision code
APPR
Product code
MFK
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
Approval of the revised protocol for the post-approval study (PAS) protocol.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
CENTURION Vision System (Active SentryTM) (K161794)Alcon Research, Ltd.2017-04-14
HyperVit Vitrectomy Probe, 23 GA, HyperVit Vitrectomy Probe, 25+, HyperVit Vitrectomy Probe, 27+ (K170520)Alcon Research, Ltd.2017-03-22
CONSTELLATION VISION SYSTEM (K141065)Alcon Research, Ltd.2014-08-22
WAVELIGHT FS200 PATIENT INTERFACE 1505 (K121031)Alcon Research, Ltd.2012-06-21
MONARCH III IOL DELIVERY SYSTEM, MONARCH III C CARTRIDGE, MONARCH III HANDPIECE (H4) (K112977)Alcon Research, Ltd.2012-03-27
27+ ULTRAVIT PROBE, 27+ FLEX-TIP LASER PROBE, 27+ ENDOILLUMINATOR PROBE, 27+ VALVED ENTRY SYSTEM, 27+ INFUSION CANNULA (K110951)Alcon Research, Ltd.2011-10-17
CLEARCUT S SAFETY KNIFE (K110166)Alcon Research, Ltd.2011-05-20
ALCON MULTI-PIRPOSE DISINFECTING SOLUTION (K102860)Alcon Research, Ltd.2011-05-10