The following data is part of a premarket notification filed by K2m, Inc. with the FDA for Cascadia Interbody System.
Device ID | K172009 |
510k Number | K172009 |
Device Name: | Cascadia Interbody System |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | K2M, Inc. 600 Hope Parkway SE Leesburg, VA 20175 |
Contact | Nancy Giezen |
Correspondent | Nancy Giezen K2M, Inc. 600 Hope Parkway SE Leesburg, VA 20175 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-07-03 |
Decision Date | 2017-12-14 |
Summary: | summary |