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 |