The following data is part of a premarket notification filed by Medicrea International with the FDA for Pass Oct Patient Specific Rods.
| Device ID | K153169 |
| 510k Number | K153169 |
| Device Name: | PASS OCT Patient Specific Rods |
| Classification | Posterior Cervical Screw System |
| Applicant | MEDICREA INTERNATIONAL 14 Porte Du Grand Lyon Neyron, FR 01700 |
| Contact | Davis Ryan |
| Correspondent | David Ryan MEDICREA INTERNATIONAL 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 | 2015-11-02 |
| Decision Date | 2016-01-29 |