The following data is part of a premarket notification filed by K2m with the FDA for Cascadia Interbody System.
Device ID | K160547 |
510k Number | K160547 |
Device Name: | Cascadia Interbody System |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | K2M 751 MILLER DR SE Leesburg, VA 20175 |
Contact | Nancy Giezen |
Correspondent | Nancy Giezen K2M 751 MILLER DR SE Leesburg, VA 20175 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-02-26 |
Decision Date | 2016-03-24 |
Summary: | summary |