The following data is part of a premarket notification filed by Facetlink Dba Linkspine with the FDA for Corticalink Spinal Fusion Platform.
Device ID | K160722 |
510k Number | K160722 |
Device Name: | CorticaLINK Spinal Fusion Platform |
Classification | Thoracolumbosacral Pedicle Screw System |
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 | NKB |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-03-16 |
Decision Date | 2016-07-07 |
Summary: | summary |