FDA 510(k) Applications Submitted by Centinel Spine, Inc.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K152211 |
08/07/2015 |
PCT System |
CENTINEL SPINE, INC. |
| K173347 |
10/25/2017 |
STALIF C FLX, STALIF M FLX, STALIF L FLX and STALIF Lateral-Oblique FLX, ACTILIF C FLX, ACTILIF M FLX, ACTILIF L FLX and ACTILIF Lateral-Oblique FLX |
Centinel Spine, Inc. |
| K150053 |
01/12/2015 |
STALIF C; STALIF C-Ti |
Centinel Spine, Inc. |
| K120819 |
03/19/2012 |
STALIF C |
CENTINEL SPINE, INC. |
| K133200 |
10/17/2013 |
STALIF C(R) |
CENTINEL SPINE, INC. |
| K133286 |
10/25/2013 |
MIDLINE (TM) |
CENTINEL SPINE, INC. |
| K141942 |
07/17/2014 |
MIDLINE II TI |
CENTINEL SPINE, INC. |
| K142079 |
07/31/2014 |
STALIF CTI, STALIF C |
CENTINEL SPINE, INC. |
| K150643 |
03/12/2015 |
Centinel Spine STALIF TT, STALIF MIDLINE, MIDLINE II, MIDLINE II-Ti |
CENTINEL SPINE, INC. |
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