The following data is part of a premarket notification filed by K2m Inc. with the FDA for Chesapeake Stabilization System.
Device ID | K142487 |
510k Number | K142487 |
Device Name: | Chesapeake Stabilization System |
Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Applicant | K2M Inc. 571 Miller Drive SE Leesburg, VA 20175 |
Contact | Nancy Giezen |
Correspondent | Nancy Giezen K2M Inc. 571 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 | 2014-09-04 |
Decision Date | 2015-05-07 |
Summary: | summary |