Medical Device Manufacturer · US , Irvine , CA

Interventional Spine, Inc. - FDA 510(k) Cleared Devices

8 submissions · 7 cleared · Since 2008

8

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Interventional Spine, Inc. Orthopedic ✕

8 devices

1-8 of 8

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