The following data is part of a premarket notification filed by Curiteva, Llc with the FDA for Curiteva Lumbar Interbody Fusion System.
Device ID | K181589 |
510k Number | K181589 |
Device Name: | Curiteva Lumbar Interbody Fusion System |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
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 | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-06-18 |
Decision Date | 2018-12-20 |
Summary: | summary |