Atlas FDA

TECHNOLAS EXCIMER LASER SYSTEM (217A AND 217Z)

FDA premarket approval P990027 · decided 2000-02-23

Approval details

PMA number
P990027
Trade name
TECHNOLAS EXCIMER LASER SYSTEM (217A AND 217Z)
Generic name
Excimer laser system
Applicant
Technolas Perfect Vision GmbH
Date received
1999-05-28
Decision date
2000-02-23
Days to decision
271 days
Decision code
APPR
Product code
LZS
Advisory committee
Ophthalmic
Expedited review
No
Location
München
Statement
APPROVAL FOR THE TECHNOLAS(R) 217A EXCIMER LASER SYSTEM. THE DEVICES IS INDICATED TO PERFORM LASER IN-SITU KERATOMILEUSIS (LASIK): 1) IN TREATMENTS FOR THE REDUCTION OR ELIMINATINO OF MYOPIA (NEARSIGHTEDNESS) FROM -1.00 TO -7.00 DIOPTERS D WITH LESS THAN -3.00 D ASTIGMATISM; 2) IN PATIENTS WITH DOCUMENTED STABILITY OF REFRACTION FOR THE PRIOR 12 MONTHS AS DEMONSTRATED BY A CHANGE IN MANIFEST REFRACTION OF LESS THAN OR EQUAL TO 0.5 D (IN BOTH CYLINDER AND SPHERE COMPONENTS); AND, 3) IN PATIENTS 2

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
VICTUS Femtosecond Laser Platform (K200724)Technolas Perfect Vision GmbH2020-09-01
VICTUS Femtosecond Laser Platform (K171014)Technolas Perfect Vision GmbH2017-10-19
VICTUS Femtosecond Laser Platform (K151161)Technolas Perfect Vision GmbH2015-06-24
VICTUS FEMTOSECOND LASER PLATFORM (K141379)Technolas Perfect Vision GmbH2015-01-16
VICTUS FEMTOSECOND LASER PLATFORM (K140615)Technolas Perfect Vision GmbH2014-07-15
VICTUS FEMTOSECOND LASER PLATFORM (K132534)Technolas Perfect Vision GmbH2014-02-14
VICTUS FEMTOSECOND LASER PLATFORM (K122386)Technolas Perfect Vision GmbH2013-02-08
VICTUS LASER PLATFORM (K120426)Technolas Perfect Vision GmbH2012-07-31