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 |