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 |