Blue Belt Technologies, Inc. announced the first NavioPFS™ unicondylar knee replacement procedure performed in the United Kingdom. The NavioPFS surgical system represents a new generation of smart instrumentation with robotic control.
Orthopaedics
Stryker Changes Executive Leadership
Just a month after taking the hot seat, Kevin Lobo has had something we Brits might call a cabinet reshuffle, bringing in a new man to replace himself in heading up the company’s vital orthopedics business.
Is It OK To Adopt A New Technique Without Some Form Of Regulatory Approval?
Medical professionals are always right. They must be, because we don’t bother to regulate their practices, let alone require formal centralised approval of new techniques prior to their introduction. Meanwhile the device industry is increasingly regulated. We ask whether this is all entirely the best way of doing things.
BioKnee May Delay Or Avoids Knee Replacement
San Francisco sportsmed surgeon Kevin Stone’s eponymous Stone Clinic has formally introduced BioKnee: A natural knee cartilage reconstruction solution clinically-proven to delay the effects of arthritis for up to 12 years.
Can Laparoscopy Concepts Work In Hip Arthroscopy?
UK based MIS device company Surgical Innovations (SI) chose last week’s International Society of Hip Arthroscopy (ISHA) meeting in Boston, at which to showcase its pre-production hip arthroscopy products.
New, Unique Trigen™ Low-profile Screw With “Captured” Head Technology From Smith & Nephew
Smith & Nephew has chosen to announce the launch of its Trigen™ Low-Profile Screw at this week’s Orthopaedic Trauma Association meeting in Minneapolis. In a press release it says Trigen is the only truly “captured” head, low-profile screw on the market.
New President And CEO For Stryker
Stryker Corporation’s Board of Directors announced today that Kevin A. Lobo has been named the Company’s President and Chief Executive Officer, effective immediately. He has also been named to the Company’s Board of Directors. Mr. Lobo joined Stryker in April 2011, and was most recently Group President of Stryker Orthopaedics.
DePuy Mitek Says New Healix Advance™ Rotator Cuff Anchors Tick All The Boxes
Orthopaedic and Sports Med company DePuy Mitek, Inc., has announced the launch of the Healix Advance™ Family of Suture Anchors, a comprehensive new system of rotator cuff anchor and instrumentation solutions. The company says its new anchor design will enable faster insertion into hard bone and maximise fixation and pull-out strength.
Endurance™ Hip Solutions System Signals DePuy Mitek’s Foray into Hip Arthroscopy
Orthopaedic and Sport Med device company DePuy Mitek, Inc.has announced the launch of Endurance Hip Solutions, a new system of instruments and devices that marks the company’s entry into the rapidly growing field of hip arthroscopy.
South Korean Knee Prosthesis Gains FDA Clearance
South Korean manufactured Lospa Knee® System from Corentec features cruciate retaining and posterior stabilised knee within a single system
S&N’s New Hinged Knee Builds on Legion™ Total Knee System Heritage
Smith & Nephew has announced the launch of its Legion™ HK Hinge Knee implant to surgeons in the US and Canada. As the first hinged knee to be designed using normal knee kinematics, the implant provides a new option for those patients facing difficult primary or revision knee surgery.
Biodegradable Metal? But (Hopefully) Not Like My First Car
Combine the strength of steel with the absorption characteristics of a polymer like PLLA and you may have a new category of implant material. So hopes Bio DG which has just been granted a patent in the area.
Biomet To Distribute Bonesupport’s Proprietary Cerament™Bone Void Filler
Biomet is to be the exclusive distributor of Bonesupport’s proprietary Cerament™ bone void filler in an agreement which spans U.S. and Canada.
LOQTEQ® Trauma Plating System Gets Initial 510(k). More To Follow
Trauma and biomaterials company aap Implantate AG. has announced that it has received 510(k) clearance from the U.S FDA for the small fragment plating line of its Loqteq® product family.
Bold Claims For CarpalFiX™ Hand & Wrist Fusion System As It Gains FDA Clearance
Extremity Medical LLC claims its device delivers superior compression and stable fixation for fusion while remaining zero profile and avoiding damage to vital articular surfaces. The system has just gained FDA clearance.
NICE Asks The Audience On Exogen
Smith & Nephew has announced that the UK’s National Institute for Health and Clinical Excellence (NICE) has issued draft guidance supporting the case for utilising the Exogen Ultrasound Bone Healing System. It’s now putting its draft findings out for consultation.