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 |