The following data is part of a premarket notification filed by K2m, Inc with the FDA for Sahara Stabilization System.
Device ID | K151481 |
510k Number | K151481 |
Device Name: | Sahara Stabilization System |
Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Applicant | K2M, INC 751 MILLER DRIVE SE Leesburg, VA 20175 |
Contact | Nancy Giezen |
Correspondent | Nancy Giezen K2M, INC 751 MILLER DRIVE SE Leesburg, VA 20175 |
Product Code | OVD |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-06-02 |
Decision Date | 2015-12-21 |
Summary: | summary |