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

Lens, Intraocular, Phakic

PMA: P030016 · Supplement: S011 · Decision Jan 14, 2009
Classifications
1
FEI Numbers
5
Registration Numbers
5

Basic Information

Device Name
Lens, Intraocular, Phakic
Trade Name
STAAR SURGICAL COLLAMER ULTRAVIOLET ABSORBING POSTERIOR CHAMBER
PMA Number
P030016
Supplement Number
S011
Device Class
FDA Class 3
Product Code
MTA
Generic Name
Lens, intraocular, phakic
Medical Specialty
Unknown
Advisory Committee
Ophthalmic
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
January 14, 2009
Date Received
October 9, 2008
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

ADDITION OF A SECOND WAX DISPENSING SYSTEM.

Classifications

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

Product Code Device Name
MTA Lens, Intraocular, Phakic