WebSep 1, 2005 · INTER FIX Threaded Fusion Device and the INTER FIX RP Threaded Fusion Device. The INTER FIX and the INTER FIX RP (Medtronic Sofamor Danek) are second-generation cylindrical, fenestrated, titanium cages that permit improved CT imaging because of the decreased wall thickness (Fig 1D). These devices can be implanted through …
Devices@FDA - Food and Drug Administration
WebDevice: INTER FIX THREADED FUSION DEVICE: Generic Name: intervertebral fusion device with bone graft, lumbar: Regulation Number: 888.3080: Applicant: SOFAMOR DANEK 1800 pyramid place memphis, TN 38132: PMA Number: P970015: Supplement Number: S028: Date Received: 07/01/2004: Decision Date: 07/19/2004: Reclassified Date 07/12/2007: WebFeb 1, 2004 · Medtronic, Inc. (NYSE:MDT), has received U.S. Food and Drug Administration (FDA) approval for the expanded use of INFUSE(R) Bone Graft with certain sizes of the INTER FIX(TM) and INTER FIX(TM) RP Threaded Fusion Devices. INFUSE Bone Graft was approved in July 2002 by the FDA for use with the LT-CAGE(R) Lumbar Tapered Fusion … brighter paths wellness and counseling
INTER FIX™ RP Threaded Fusion Device - MEDTRONIC SOFAMOR …
WebA device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). WebThe Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical devices that have Unique Device Identifiers (UDI). WebBrand Name: INTER FIX™ RP Threaded Fusion Device Version or Model: 9011426 Commercial Distribution Status: In Commercial Distribution Catalog Number: Company Name: MEDTRONIC SOFAMOR DANEK, INC. Primary DI Number: 00673978957388 Issuing Agency: GS1 Commercial Distribution End Date: Device Count: 1 Labeler D-U-N-S® … can you drink alcohol on ciprofloxacin