FDA PMA FDA Class 3 Approved 🇺🇸 United States

Lens, Intraocular, Toric Optics

PMA: P030002 · Supplement: S034 · Decision Jun 2, 2015
Classifications
1
FEI Numbers
19
Registration Numbers
19

Basic Information

Device Name
Lens, Intraocular, Toric Optics
Trade Name
TRULIGN TORIC POSTERIOR CHAMBER INTRAOCULAR LENS
PMA Number
P030002
Supplement Number
S034
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
Approved
Decision Code
APPR
Decision Date
June 2, 2015
Date Received
April 1, 2015
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Postapproval Study Protocol - OSB
Expedited Review
N

Advisory Committee Statement

APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL.

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