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| Trade Name | MEDITEC MEL 80 EXCIMER LASER SYSTEM |
| Classification Name | excimer laser system |
| Generic Name | ophthalmic medical laser system(193 nanometer wavelenght) |
| Applicant | CARL ZEISS, INC. |
| PMA Number | P060004 |
| Supplement Number | S001 |
| Date Received | 12/28/2007 |
| Decision Date | 03/28/2011 |
| Product Code | |
| Docket Number | 11M-0256 |
| Notice Date | 04/25/2011 |
| Advisory Committee |
Ophthalmic |
| Clinical Trials |
NCT00762281
|
| Supplement Type | panel track |
| Supplement Reason | change design/components/specifications - other |
| Expedited Review Granted? | No |
| Combination Product |
No
|
| Information About: |
Labeling, Approval Order, Summary of Safety and Effectiveness |
Approval Order Statement Approval for the mel 80 excimer laser system. This device uses an optical zone of 6. 0 to 6. 5 mm in diameter and a transition zone of 2. 0 to 4. 0 mm for a total ablation diameter of 10. 0 mm, and is indicated for primary laser assisted in situ keratomileusis (lasik) treatments for: 1) the reduction or elimination of naturally-occurring hyperopia of less than or equal to +5. 0 d with or without refractive astigmatism of > +0. 5 and <= +3. 0d, with a maximum mrse of +5. 0d; 2) in patients who are 21 years of age or older; and 3) with documentation of stable manifest refraction over the past year as demonstrated by change in sphere and cylinder of <= 0. 5d. |
| Approval Order |
Approval Order
|