The following data is part of a premarket notification filed by K2m, Inc. with the FDA for Chesapeake Spinal System.
Device ID | K133494 |
510k Number | K133494 |
Device Name: | CHESAPEAKE SPINAL SYSTEM |
Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Applicant | K2M, INC. 751 MILLER DR. SE Leesburg, VA 20175 |
Contact | Nancy Giezen |
Correspondent | Nancy Giezen K2M, INC. 751 MILLER DR. 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 | 2013-11-14 |
Decision Date | 2014-06-10 |
Summary: | summary |