TECHNOLAS(R)217A OPHTHALMIC EXCIMER LASER SYSTEM

Excimer Laser System

FDA Premarket Approval P990027 S003

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

Approval to add an active eyetracker as an accessory to the laser system.

DeviceTECHNOLAS(R)217A OPHTHALMIC EXCIMER LASER SYSTEM
Classification NameExcimer Laser System
Generic NameExcimer Laser System
ApplicantTECHNOLAS PERFECT VISION GMBH
Date Received2001-04-27
Decision Date2001-09-25
PMAP990027
SupplementS003
Product CodeLZS
Advisory CommitteeOphthalmic
Supplement TypeNormal 180 Day Track
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product No
Applicant Address TECHNOLAS PERFECT VISION GMBH messerschmittstr 1 + 3 munchen 80992

Supplemental Filings

Supplement NumberDateSupplement Type
P990027Original Filing
S020 2015-10-07 30-day Notice
S019 2014-01-31 30-day Notice
S018 2012-05-01 Normal 180 Day Track
S017 2012-04-26 Real-time Process
S016 2010-09-17 135 Review Track For 30-day Notice
S015 2010-06-29 Normal 180 Day Track
S014
S013 2009-10-01 Real-time Process
S012 2009-05-15 Normal 180 Day Track No User Fee
S011 2008-09-03 Normal 180 Day Track
S010 2008-08-11 Normal 180 Day Track
S009 2006-12-19 Normal 180 Day Track
S008
S007 2004-09-10 Normal 180 Day Track
S006 2002-07-18 Panel Track
S005 2002-01-31 Normal 180 Day Track
S004 2001-12-14 Panel Track
S003 2001-04-27 Normal 180 Day Track
S002 2000-11-24 Panel Track
S001 2000-10-13 Normal 180 Day Track

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