Seaspine, Inc. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
FDA 510(k) cleared devices by Seaspine, Inc. Orthopedic ✕
26 devices
Cleared
Aug 03, 2023
NorthStar OCT System
Orthopedic
58d
Cleared
Mar 23, 2015
Integra Laminoplasty System
Orthopedic
28d
Cleared
Dec 18, 2014
SeaSpine Spacer System - (Hollywood, Pacifica, Redondo, Ventura)...
Orthopedic
105d
Cleared
May 01, 2014
INTEGRA EXPANDABLE INTERVEREBRAL BODY FUSION DEVICE (IBD) SYSTEM
Orthopedic
175d
Cleared
Nov 18, 2013
INTEGRA FACET FIXATION SYSTEM
Orthopedic
67d
Cleared
Sep 04, 2013
INTEGRA INTERSPINOUS PROCESS SYSTEM
Orthopedic
429d
Cleared
May 09, 2013
INTEGRA LAMINOPLASTY SYSTEM
Orthopedic
44d
Cleared
Dec 12, 2012
MALIBU SPINAL SYSTEM WITH THE DAYTONA DEFORMITY SYSTEM
Orthopedic
111d
Cleared
Jan 25, 2012
CARDIFF ANTERIOR CERVICAL PLATE SYSTEM
Orthopedic
177d
Cleared
May 12, 2011
SEASPINE SPACER SYSTEM
Orthopedic
297d
Cleared
Jan 27, 2011
REDONDO-L
Orthopedic
80d
Cleared
Apr 13, 2010
ZUMA-C
Orthopedic
238d