The following data is part of a premarket notification filed by Nuvasive, Incorporated with the FDA for Nuvasive Tlx Interbody System.
Device ID | K171633 |
510k Number | K171633 |
Device Name: | NuVasive TLX Interbody System |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | NuVasive, Incorporated 7475 Lusk Blvd. San Diego, CA 92121 |
Contact | Cynthia Adams |
Correspondent | Cynthia Adams NuVasive, Incorporated 7475 Lusk Blvd. San Diego, CA 92121 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-06-02 |
Decision Date | 2017-09-28 |
Summary: | summary |