The following data is part of a premarket notification filed by Life Spine, Inc with the FDA for Pro-link Cervical Spacer System.
| Device ID | K121151 |
| 510k Number | K121151 |
| Device Name: | PRO-LINK CERVICAL SPACER SYSTEM |
| Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
| Applicant | LIFE SPINE, INC 2401 W. HASSELL RD SUITE 1535 Hoffman Estates, IL 60169 |
| Contact | Randy Lewis |
| Correspondent | Randy Lewis LIFE SPINE, INC 2401 W. HASSELL RD SUITE 1535 Hoffman Estates, IL 60169 |
| Product Code | OVE |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-04-16 |
| Decision Date | 2012-11-16 |
| Summary: | summary |