The following data is part of a premarket notification filed by Facetlink Dba Linkspine with the FDA for Vertebralink Fusion Platform.
Device ID | K162693 |
510k Number | K162693 |
Device Name: | VertebraLINK Fusion Platform |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | FACETLINK DBA LINKSPINE 101 ROUNDHILL DRIVE Rockaway, NJ 07866 |
Contact | Massimo Calafiore |
Correspondent | Kenneth C. Maxwell EMPIRICAL TESTING CORP. 4628 NORTHPARK DRIVE Colorado Springs, CO 80918 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-09-27 |
Decision Date | 2017-03-29 |
Summary: | summary |