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 |