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BioWorld - Monday, May 11, 2026
Home » Topics » Disease categories and therapies » Orthopedics

Orthopedics
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BioWorld MedTech’s Orthopedics Extra for June 24, 2020

June 24, 2020
By Holland Johnson
Keeping you up to date on recent developments in orthopedics, including: Nuclear softening allows cells to move into dense tissue, encouraging injury repair; 3D X-ray reveals secrets from inside bones; Fantastic muscle proteins and where to find them.
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Naviswiss device used in surgery

FDA gives nod to Naviswiss’ hip surgery navigation system

June 19, 2020
By Meg Bryant
Smart assisted surgery company Naviswiss AG, of Brugg, Switzerland, has gained U.S. FDA clearance for its miniature navigation technology for hip replacement surgery. The hand-held system, with an open platform that supports all implant vendors, is being offered on a fee per-use basis.
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Syringe with Osteo3 Zp putty and packaging

Sirakoss scores FDA nod for nanoparticle synthetic bone graft substitute

June 18, 2020
By Nuala Moran
LONDON – Sirakoss Ltd. has received FDA 510(k) clearance for its nanoparticle synthetic bone graft substitute, after showing the ready-to-use putty is equivalent to the CE-approved dry formulation. Rather than granules that are mixed with a patient’s blood before administration, the inorganic calcium phosphate-based Osteo3 Zp putty consists of the granules suspended in a fully synthetic resorbable carrier.
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BioWorld MedTech’s Orthopedics Extra for June 17, 2020

June 17, 2020
By Holland Johnson
Keeping you up to date on recent developments in orthopedics, including: Osteoporosis treatment also may protect against pneumonia; Study finds similar short-term outcomes after common MI spine procedures; New biomaterial has potential to repair damaged bone with lower risk of inflammation; Diabetics face greater risk of bone fractures.
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Components of the Go-2 system

Gtx Medical receives breakthrough device designation for implanted spinal stimulation system

June 10, 2020
By Annette Boyle
The U.S. FDA granted Gtx Medical BV a breakthrough device designation for its implantable Go-2 Targeted Epidural Spinal Stimulation (TESS) system. The device enabled patients who had sustained traumatic spinal cord injuries to regain voluntary control over previously paralyzed muscles and walk again four or more years after paralysis, according to a study previously published in Nature.
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BioWorld MedTech’s Orthopedics Extra for June 10, 2020

June 10, 2020
By Holland Johnson
Keeping you up to date on recent developments in orthopedics, including: Researchers restore injured man's sense of touch using brain-computer interface technology; Down to the bone: Understanding how bone-dissolving cells are generated; Improved MRI scans could aid in development of arthritis treatments.
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BioWorld MedTech’s Orthopedics Extra for June 3, 2020

June 3, 2020
By Holland Johnson
Keeping you up to date on recent developments in orthopedics, including: IMPACT study shows 25% reduction in health care costs associated with earlier prosthetic care; Human growth hormone treatment after ACL injury may prevent loss of muscle strength; Osteoporosis treatment may also protect against pneumonia.
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Image from pilot animal study

Launchpad Medical nabs $1.8M grant for pivotal animal study of dental bone graft solution

June 2, 2020
By Meg Bryant
Lowell, Mass.-based startup Launchpad Medical LLC has picked up an additional $1.8 million grant from the Michigan-Pittsburgh-Wyss Regenerative Medicine Resource Center to advance the development of its bone graft solution. The company plans to use the funds to conduct a pivotal animal study of the injectable biomaterial, which will pave the way for a U.S. FDA-approved clinical trial.
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BioWorld MedTech’s Orthopedics Extra for May 27, 2020

May 27, 2020
By Holland Johnson
Keeping you up to date on recent developments in orthopedics, including: Cell 'pores' discovery gives hope to millions of brain and spinal cord injury patients; Little skates could hold the key to cartilage therapy in humans; Spinal cord injury increases risk for mental health disorders.
Read More
Orthocell CEO with employees in the lab

Australia’s Orthocell submits 510(k) for Celgro regenerative collagen medical device

May 22, 2020
By Tamra Sami
PERTH, Australia – Perth-based regenerative medicine company Orthocell Ltd. has submitted a 510(k) application to the U.S. FDA for its Celgro collagen medical device for dental guided bone and soft tissue regeneration applications. The submission follows positive results from an FDA-guided bone regeneration study, which is a key component toward the goal of gaining U.S. marketing approval.
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