The following data is part of a premarket notification filed by Additive Implants, Llc with the FDA for Cervical Spacer.
Device ID | K182477 |
510k Number | K182477 |
Device Name: | Cervical Spacer |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
Applicant | Additive Implants, LLC 3101 E. Shea Blvd, Suite 114 Pheonix, AZ 85028 |
Contact | Jeff Horn |
Correspondent | Karen E. Warden BackRoads Consulting 12520 Heath Road Chesterland, OH 44026 |
Product Code | ODP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-09-10 |
Decision Date | 2019-01-28 |
Summary: | summary |