The following data is part of a premarket notification filed by Orthofix Inc. with the FDA for Centurion Poct System.
Device ID | K180025 |
510k Number | K180025 |
Device Name: | Centurion POCT System |
Classification | Posterior Cervical Screw System |
Applicant | Orthofix Inc. 3451 Plano Parkway Lewisville, TX 75056 |
Contact | Jacki Koch |
Correspondent | Jacki Koch Orthofix Inc. 3451 Plano Parkway Lewisville, TX 75056 |
Product Code | NKG |
CFR Regulation Number | 888.3075 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-01-03 |
Decision Date | 2018-01-22 |
Summary: | summary |