Centinel Spine, Inc. - FDA 510(k) Cleared Devices
Recent clearances: 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
10
Total
10
Cleared
0
Denied
FDA 510(k) Regulatory Record - Centinel Spine, Inc. Orthopedic ✕
10 devices
Cleared
May 08, 2018
STALIF C FLX, STALIF M FLX, STALIF L FLX and STALIF Lateral-Oblique FLX,...
Orthopedic
195d
Cleared
Dec 01, 2015
PCT System
Orthopedic
116d
Cleared
Jun 24, 2015
STALIF C
Orthopedic
163d
Cleared
Jun 08, 2015
Centinel Spine STALIF TT, STALIF MIDLINE, MIDLINE II, MIDLINE II-Ti
Orthopedic
88d
Cleared
Nov 07, 2014
MIDLINE II TI
Orthopedic
113d
Cleared
Oct 24, 2014
STALIF CTI, STALIF C
Orthopedic
85d
Cleared
May 08, 2014
STALIF C(R)
Orthopedic
203d
Cleared
Jan 09, 2014
MIDLINE (TM)
Orthopedic
76d
Cleared
Aug 28, 2013
STALIF X
Orthopedic
187d
Cleared
Aug 31, 2012
STALIF C
Orthopedic
165d