The following data is part of a premarket notification filed by Nuvasive, Incorporated with the FDA for Expandable Lumbar Interbody System.
Device ID | K130820 |
510k Number | K130820 |
Device Name: | EXPANDABLE LUMBAR INTERBODY SYSTEM |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | NUVASIVE, INCORPORATED 7475 LUSK BOULEVARD San Diego, CA 92121 |
Contact | Jeremy Markovich |
Correspondent | Jeremy Markovich NUVASIVE, INCORPORATED 7475 LUSK BOULEVARD 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 | 2013-03-25 |
Decision Date | 2013-08-08 |
Summary: | summary |