The following data is part of a premarket notification filed by Orthofix Inc. with the FDA for Cervical Stand Alone System.
Device ID | K161280 |
510k Number | K161280 |
Device Name: | Cervical Stand Alone System |
Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
Applicant | Orthofix Inc. 3451 Plano Parkway Lewisville, TX 75056 |
Contact | Natalia Volosen |
Correspondent | Natalia Volosen Orthofix Inc. 3451 Plano Parkway Lewisville, TX 75056 |
Product Code | OVE |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-05-06 |
Decision Date | 2016-06-17 |
Summary: | summary |