The following data is part of a premarket notification filed by Curiteva, Inc. with the FDA for Curiteva Pedicle Screw System.
Device ID | K191810 |
510k Number | K191810 |
Device Name: | Curiteva Pedicle Screw System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Curiteva, Inc. 25127 Will McComb Drive Tanner, AL 35671 |
Contact | Eric Linder |
Correspondent | Eric Linder Curiteva, Inc. 25127 Will McComb Drive Tanner, AL 35671 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-07-05 |
Decision Date | 2019-08-28 |