The following data is part of a premarket notification filed by Tyber Medical Llc with the FDA for Tyber Medical Pt Interbody Spacer System.
Device ID | K172185 |
510k Number | K172185 |
Device Name: | Tyber Medical PT Interbody Spacer System |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
Applicant | Tyber Medical LLC 83 South Commerce Way, Bethlehem, PA 18017 |
Contact | Mark F. Schenk |
Correspondent | Mark F. Schenk Tyber Medical LLC 83 South Commerce Way, Suite 310 Bethlehem, PA 18017 |
Product Code | ODP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-07-20 |
Decision Date | 2017-12-21 |
Summary: | summary |