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Medtronic catalyft ls

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). WebK214011: 02/09/2024 anteralign spinal system with titan nanolock surface technology: Medtronic Sofamor Danek USA K214010: 04/12/2024 catalyft ls expandable interbody system with titan nanolock surface technology: Medtronic Sofamor Danek USA, Inc. K223153 clover printer paper By Medtronic FEATURING Samuel Kalb-Goldsmit …

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WebMedtronic Canada - Patient Services. 1-888-660-4616 (Toll Free) 99 Hereford Street Brampton, Ontario L6Y 0R3 [email protected] WebMEDTRONIC SOFAMOR DANEK, INC. (8) Brand Name. Catalyft™ LS Expandable Interbody System (8) GMDN Term. Bone-screw internal spinal fixation system, sterile (8) FDA Product Code Name. Appliance, fixation, spinal intervertebral body (8) ... humanity\\u0027s ls https://departmentfortyfour.com

Catalyft Interbody System - Spine Products Medtronic

WebCatalyft™ PL Expandable Interbody System implants are interbody devices and are intended to stabilize the operative area during the fusion process. Retrieved devices … Web17 aug. 2024 · Medtronic: Catalyft PL40 SPINEMarketGroup 1.13K subscribers Subscribe 2.3K views 1 year ago For Educational purpose only! No copyright infringement intended … WebSPACER 6069076 CATALYFT PL40 LONG 7MM Medical Device Identification Catalyft PL Expandable Interbody System GUDID 00763000246792 SPACER 6069076 CATALYFT PL40 LONG 7MM MEDTRONIC SOFAMOR DANEK, INC. FDA.report › GUDID › MEDTRONIC SOFAMOR DANEK, INC. › 00763000246792 humanity\\u0027s lr

Spinal & Orthopaedic Products Medtronic

Category:DEVICE: Catalyft PL Expandable Interbody System (00763000246693)

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Medtronic catalyft ls

DEVICE: Catalyft PL Expandable Interbody System (00763000246693)

WebMEDTRONIC SOFAMOR DANEK, INC. (26) Brand Name. Catalyft™ LS Expandable Interbody System (21) Anteralign Spinal System with Titan nanoLock Surface technology … WebBrand Name:Catalyft™ LS Expandable Interbody System Version or Model:981000007 Commercial Distribution Status:In Commercial Distribution Catalog Number: Company …

Medtronic catalyft ls

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WebCompany Name. MEDTRONIC SOFAMOR DANEK, INC. (9) Brand Name. Catalyft™ LS Expandable Interbody System (5) Anteralign Spinal System with Titan nanoLock Surface technology (4) Web販売名: 低侵襲脊椎手術用器械. 医療機器届出番号: 13B1X10244S00045. 製造販売業者：日本メドトロニック株式会社. 販売名: ステルスマイダス 電動式ハンドピース. 医療機器認証番号：228ADBZX00127000. 販売名: マイダスレックス レジェンド アタッチメント. 医療機器 ...

WebThe Catalyft™ LS Expandable Interbody system consists of implants, instruments, and trays. The implants are provided sterile and are intended to be surgically implanted … WebMEDTRONIC SOFAMOR DANEK, INC. (13) Brand Name. Catalyft™ LS Expandable Interbody System (5) Sovereign™ Spinal System (4) ...

WebCatalyft LS Expandable Interbody System: Applicant: Medtronic Sofamor Danek USA, Inc. 1800 Pyramid Place: Memphis, TN 38132 Applicant Contact: Madhuvanthi … WebCD Horizon™ Astute™ Spinal System (24) CD Horizon™ ModuLeX™ Spinal System (119) CD Horizon™ Modular 5.5/6.0mm Spinal System (5) CD Horizon™ Spinal System (30) CD® Spinal System (9) CD™ SPINAL SYSTEM (1) CENTERPIECE™ Plate Fixation System (60) CG FUTURE® (42) CG FUTURE™ (15)

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).

WebCatalyft™ LS Expandable Interbody System GUDID 00763000465896 SPACER 981025525 10MM ANT EXPANDABLE MD MEDTRONIC SOFAMOR DANEK, INC. FDA.report › GUDID › MEDTRONIC SOFAMOR DANEK, INC. › 00763000465896. humanity\\u0027s m0WebMEDTRONIC SOFAMOR DANEK, INC. (5) Brand Name. Catalyft™ LS Expandable Interbody System (5) GMDN Term. Orthopaedic implant inserter/extractor, reusable (5) FDA Product Code Name. Intervertebral fusion device with bone graft, lumbar (5) Intervertebral fusion device with integrated fixation, lumbar (5) humanity\u0027s mWebThe Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical devices that have Unique … humanity\u0027s m1