Meditech spine llc
WebThe following data is part of a premarket notification filed by Meditech Spine, Llc with the FDA for Cure™ Opel-c Plate System. Pre-market Notification Details. Device ID: K181543: 510k Number: K181543: Device Name: Cure™ OPEL-C Plate System: Classification: Appliance, Fixation, Spinal Intervertebral Body: WebMeditech Spine, LLC 220 followers on LinkedIn. Market forces should drive innovation and not regulatory constraints. A large part of this innovation comes from the end users. We must continue to adapt and create within the competitive landscape, and surgeons will help drive our ingenuity.
Meditech spine llc
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WebThis page includes the latest FDA filings for Meditech Spine L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations. FDA Registration (s) FDA Filings Related Finance Registrations © 2024 FDA.report WebSPINAL IMPLANT ALIGNMENT GUIDE SYSTEMS - MediTech Spine, LLC Title: SPINAL IMPLANT ALIGNMENT GUIDE SYSTEMS United States Patent Application 20140156008 Kind Code: A1 Abstract: Systems for improved methods of performing a spinal fusion procedure that include an implant having an alignment guide system.
WebTPLC - Total Product Life Cycle Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products TPLC - Total Product Life... WebMeditech Spine, LLC, is a growing spinal implant company that currently partners with leaders in the industry to design, develop, and distribute implant devices that make a positive difference in the market. Meditech's pursuit of novel and innovative technologies drives the design and development team.
WebMEDITECH SPINE, LLC. (Atlanta, GA, US) International Classes: A61B17/80; A61B17/70. Claims: What is claimed is: 1. A locking bone plate apparatus comprising a bone plate, the bone plate comprising: a screw through-hole configured to receive a bone screw; a locking bore comprising a cavity in a superior surface of the bone plate; and a ... Web29 jan. 2024 · Meditech Spine, LLC 235 followers on LinkedIn. Market forces should drive innovation and not regulatory constraints. A large part of this innovation comes from the …
Web29 jun. 2024 · ATLANTA, June 29, 2024 /PRNewswire/ -- Meditech Spine, LLC, announced today it has received 510 (k) clearance for its CURE Lumbar Plating (LP) System from …
WebMeditech Spine, LLC Bruce Dunaway Chief Design Engineer 1447 Peachtree Street NE Suite 440 Atlanta, Georgia 30309 Re: K180090 Trade/Device Name: Cure™ Lumbar Plate System Regulation Number: 21 CFR 888.3060 Regulation Name: Spinal Intervertebral Body Fixation Orthosis Regulatory Class: Class II Product Code: KWQ Dated: March 29, 2024 cooper hale hearingWeb18 sep. 2024 · Meditech's belief in the spinal marketplace is to value and honor their partners and all who are touched by their interactions in the development and distribution process so that each... cooper hafenWeb13 jul. 2024 · At Meditech Spine, our goal has always been to work with leaders in the industry and we are excited about continuing our partnership under the global Spineart … family word scramble printablefamily word search printable freeWebThe Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical devices that have Unique Device Identifiers (UDI). family words etWebThe following data is part of a premarket notification filed by Meditech Spine, Llc with the FDA for Cure™ Lumbar Plate System. Pre-market Notification Details. Device ID: K201136: 510k Number: K201136: Device Name: Cure™ Lumbar Plate System: Classification: Appliance, Fixation, Spinal Intervertebral Body: family word search freeWeb1 jun. 2024 · Meditech Spine, LLC, is a growing spinal implant company that currently partners with leaders in the industry to design, develop, and distribute implant devices … family word search puzzle printable