The following data is part of a premarket notification filed by Neuropro Spinal Jaxx, Inc. with the FDA for Spinal Jaxx Interbody Fusion Device.
| Device ID | K152501 |
| 510k Number | K152501 |
| Device Name: | Spinal Jaxx Interbody Fusion Device |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | NEUROPRO SPINAL JAXX, INC. 4707 GREENLEAF CT., STE. C Modesto, CA 95356 |
| Contact | Benjamin J. Remington |
| Correspondent | Rich Jansen SILVER PINE CONSULTING, LLC. 11821 BRAMBLE COVE DRIVE Ft. Myers, FL 33905 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-09-01 |
| Decision Date | 2016-06-29 |
| Summary: | summary |