The following data is part of a premarket notification filed by Medicrea International with the FDA for Pass Oct Spinal System.
| Device ID | K121979 |
| 510k Number | K121979 |
| Device Name: | PASS OCT SPINAL SYSTEM |
| Classification | Appliance, Fixation, Spinal Interlaminal |
| Applicant | MEDICREA INTERNATIONAL 14 PORTE DU GRAND LYON Neyron, FR 01700 |
| Contact | Laura Aviron-violet |
| Correspondent | Laura Aviron-violet MEDICREA INTERNATIONAL 14 PORTE DU GRAND LYON Neyron, FR 01700 |
| Product Code | KWP |
| CFR Regulation Number | 888.3050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-07-06 |
| Decision Date | 2013-03-21 |
| Summary: | summary |