The following data is part of a premarket notification filed by Curiteva, Llc with the FDA for Curiteva Cervical Interbody Fusion System.
Device ID | K181261 |
510k Number | K181261 |
Device Name: | Curiteva Cervical Interbody Fusion System |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
Applicant | Curiteva, LLC 25127 Will McComb Drive Suite 100 Tanner, AL 35671 |
Contact | Eric Linder |
Correspondent | Eric Linder Curiteva, LLC 25127 Will McComb Drive Suite 100 Tanner, AL 35671 |
Product Code | ODP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-05-11 |
Decision Date | 2018-07-09 |
Summary: | summary |