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FDA 510(k) Applications Submitted by JANE METCALF
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160464
02/19/2016
Opticage(R) Expandable Interbody Fusion Device
INTERVENTIONAL SPINE, INC.
K140716
03/21/2014
OPTICAGE EXPANDABLE INTERBODY FUSION DEVICE
INTERVENTIONAL SPINE, INC.
K141313
05/20/2014
REVERSE MEDICAL MICRO VASCULAR PLUG SYSTEM
REVERSE MEDICAL CORPORATION
K152156
08/03/2015
Opticage Expandable Interbody Fusion Device
INTERVENTIONAL SPINE, INC.
K132479
08/08/2013
OPTICAGE INTERBODY FUSION DEVICE, MODEL 9080-00
INTERVENTIONAL SPINE, INC.
K182211
08/15/2018
Aurora Surgiscope System
Rebound Therapeutics Corporation
K133583
11/21/2013
OPTICAGE INTERBODY FUSION DEVICE, MODEL SERIES 9070
INTERVENTIONAL SPINE, INC.
K113527
11/30/2011
OPTICAGE INTERBODY FUSION DEVICE
INTERVENTIONAL SPINE, INC.
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