FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Lens, Intraocular, Toric Optics

PMA: P030002 · Supplement: S030 · Decision Mar 24, 2014
Classifications
1
FEI Numbers
19
Registration Numbers
19

Basic Information

Device Name
Lens, Intraocular, Toric Optics
Trade Name
CRYSTALENS ACCOMMODATING INTRAOCULAR LENS AND TRULIGN TORIC INTRAOCULAR LENS
PMA Number
P030002
Supplement Number
S030
Device Class
FDA Class 3
Product Code
MJP
Generic Name
LENS, INTRAOCULAR, TORIC OPTICS
Regulation Number
886.3600
Medical Specialty
Ophthalmic
Advisory Committee
Ophthalmic
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
March 24, 2014
Date Received
February 24, 2014
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

ADDITIONAL HAPTIC SUPPLIER BE USED.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MJP Lens, Intraocular, Toric Optics