The following data is part of a premarket notification filed by Medicrea International S.a. with the FDA for Pass Oct Spinal System.
| Device ID | K150918 |
| 510k Number | K150918 |
| Device Name: | PASS OCT Spinal System |
| Classification | Posterior Cervical Screw System |
| Applicant | MEDICREA INTERNATIONAL S.A. 14 PORTE DU GRAND LYON Neyron, FR 01700 |
| Contact | Jean-denys Marechal |
| Correspondent | Jean-denys Marechal MEDICREA INTERNATIONAL S.A. 14 PORTE DU GRAND LYON Neyron, FR 01700 |
| Product Code | NKG |
| CFR Regulation Number | 888.3075 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-04-06 |
| Decision Date | 2015-10-16 |
| Summary: | summary |