The following data is part of a premarket notification filed by Spinefrontier, Inc. with the FDA for Spinefrontier Pedfuse Pedicle Screw System.
Device ID | K123164 |
510k Number | K123164 |
Device Name: | SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEM |
Classification | Orthosis, Spondylolisthesis Spinal Fixation |
Applicant | SPINEFRONTIER, INC. 500 CUMMINGS CENTER SUITE 3500 Beverly, MA 01915 |
Contact | Fredy H Varela |
Correspondent | Fredy H Varela SPINEFRONTIER, INC. 500 CUMMINGS CENTER SUITE 3500 Beverly, MA 01915 |
Product Code | MNH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-10-09 |
Decision Date | 2013-02-15 |
Summary: | summary |