Interventional Spine, Inc. is one of 18531 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Interventional Spine, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Opticage(R) Expandable Interbody Fusion Device, Opticage Expandable Interbody Fusion Device, OPTICAGE EXPANDABLE INTERBODY FUSION DEVICE
8
Total
7
Cleared
0
Denied
Interventional Spine, Inc. has 7 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 7 cleared submissions from 2008 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Interventional Spine, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Interventional Spine, Inc.
8 devices
Cleared
Apr 04, 2016
Opticage(R) Expandable Interbody Fusion Device
Orthopedic
45d
Cleared
Oct 19, 2015
Opticage Expandable Interbody Fusion Device
Orthopedic
77d
Cleared
Nov 24, 2014
OPTICAGE EXPANDABLE INTERBODY FUSION DEVICE
Orthopedic
248d
Cleared
Feb 10, 2014
OPTICAGE INTERBODY FUSION DEVICE, MODEL SERIES 9070
Orthopedic
81d
Cleared
Sep 19, 2013
OPTICAGE INTERBODY FUSION DEVICE, MODEL 9080-00
Orthopedic
42d
Cleared
Jan 20, 2012
OPTICAGE INTERBODY FUSION DEVICE
Orthopedic
51d
Cleared
Jun 11, 2009
PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER
Orthopedic
80d
Cleared
Dec 12, 2008
SINGLE USE PERPOS PLS SYSTEM, 4.5 BONE-LOK PLS IMPLANT
Orthopedic
80d