The following data is part of a premarket notification filed by Danek Medical, Inc. with the FDA for Luque Iii Spinal System And Luque Mini-set.
| Device ID | K890192 |
| 510k Number | K890192 |
| Device Name: | LUQUE III SPINAL SYSTEM AND LUQUE MINI-SET |
| Classification | Appliance, Fixation, Spinal Interlaminal |
| Applicant | DANEK MEDICAL, INC. 3092 DIRECTOR'S ROW Memphis, TN 38131 |
| Contact | Frank M Lewis |
| Correspondent | Frank M Lewis DANEK MEDICAL, INC. 3092 DIRECTOR'S ROW Memphis, TN 38131 |
| Product Code | KWP |
| CFR Regulation Number | 888.3050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-01-18 |
| Decision Date | 1990-01-04 |