The following data is part of a premarket notification filed by Precision Spine, Inc. with the FDA for Sure-lok C Extended Tab Pedicle Screw System.
Device ID | K141397 |
510k Number | K141397 |
Device Name: | SURE-LOK C EXTENDED TAB PEDICLE SCREW SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | PRECISION SPINE, INC. 2050 EXECUTIVE DRIVE Pearl, MS 39208 |
Contact | Michael C Dawson |
Correspondent | Michael C Dawson PRECISION SPINE, INC. 2050 EXECUTIVE DRIVE Pearl, MS 39208 |
Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-05-28 |
Decision Date | 2014-06-26 |
Summary: | summary |