Atlas FDA

TECNIS Family of 1-piece IOLs packaged in the Daisy Wheel Configuration

FDA premarket approval P980040/S141 · decided 2021-07-28

Approval details

PMA number
P980040
Supplement
S141
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
TECNIS Family of 1-piece IOLs packaged in the Daisy Wheel Configuration
Generic name
intraocular lens
Applicant
Johnson & Johnson Surgical Vision, Inc.
Date received
2021-07-06
Decision date
2021-07-28
Days to decision
22 days
Decision code
OK30
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Irvine, CA
Statement
Slight increase to the lower tolerance for the ring height for the lens insert of the daisy-wheel package configuration for one-piece acrylic IOLs.

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