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FDA Approves 7D Surgical's Cranial Surgery
7D Surgical received 510(k) clearance from the FDA for its Cranial Module, a step toward launching the company's Machine-vision Image Guided Surgery system for cranial surgery throughout the U.S., according to Markets Insider. - 8/14/18 -
28 spine devices receive FDA 510(k) clearance in July
28 spine devices receive FDA 510(k) clearance in July - 8/13/18 -
Smith & Nephew stock sees downgrade over surgical robots market concerns
UBS downgraded Smith & Nephew's stock from "neutral" to "buy" after apprehensions about the company's control over the surgical robots market, according to Proactive Investors. - 8/13/18 -
3 things to know about the global interbody fusion cage market
The global interbody fusion cage market is projected grow at a 3.4 percent compound annual growth rate to reach $2.31 billion by 2023, according to a ResearchAndMarkets.com report. - 8/10/18 -
Spinal decompression therapy on the go: 3 questions with VerteCore Technologies' Paul Leake
Paul Leake is the co-founder and managing director of VerteCore Technologies, a medical device company that develops mobile decompression devices for the orthopedic market. - 8/10/18 -
Wearable medical devices market to be worth $10B by 2023: 3 report takeaways
A new Transparency Market Research report estimates the wearable devices market, including wearable vital sign monitors and obstetric devices, will be worth $10 billion by the end of 2023. - 8/9/18 -
3 insights into medical device reimbursement challenges
Infiniti Research, a market intelligence solutions provider, outlined the medical reimbursement challenges medical device companies face. - 8/9/18 -
OrthoPediatrics revenue increases 27.7% to $15.1M in Q2: 5 details
OrthoPediatrics released its 2018 second quarter financial results. - 8/9/18 -
Xtant Medical net sales decrease 12.6% in Q2: 5 things to know
Xtant Medical net sales decrease 12.6% in Q2: 5 things to know - 8/8/18 -
Mazor Robotics, Zimmer Biomet, NuVasive & more: 11 device company key notes
Here are 11 key notes from orthopedic and spine device companies in the past week. - 8/8/18 -
ORHub names interim CFO & 5 more mid-year updates
HIPAA compliant software company ORHub continued to innovate its technology with a focus on sales and marketing in the first half of 2018. - 8/8/18 -
Where Orthofix is with the Spinal Kinetics integration, what happened with extremities sales & more: 7 key quotes
Where Orthofix is with the Spinal Kinetics integration, why extremities sales were down & more: 7 key quotes - 8/8/18 -
23 commercial health plans now cover SI-BONE's iFuse Implant System
SI-BONE's iFuse Implant System is now exclusively covered by 23 commercial health plans. - 8/7/18 -
Orthofix Q2 sales spike 2.4% to $111.5M: 5 observations
Orthofix released its 2018 second quarter financial results. - 8/7/18 -
44 orthopedic, spine devices receive FDA 510(k) clearance in July
The FDA cleared 44 orthopedic-and spine-related devices in July 2018. - 8/7/18 -
UnitedHealthcare to cover lumbar total disc replacement for 16M+ members: 3 things to know
UnitedHealthcare issued positive medical policy for lumbar total disc replacement. - 8/7/18 -
Fuse Medical completes Maxim Surgical acquisition
Fuse Medical acquired Maxim Surgical, effective Aug. 1. - 8/6/18 -
Alphatec sets sights on 12 new product launches: 3 things to know about the rest of the year
Alphatec sets sights on 12 new product launches: 3 things to know about the rest of the year - 8/6/18 -
Zimmer Biomet names 2 industry veterans to board of directors — 4 things to know
Zimmer Biomet appointed Maria Teresa Hilado and Syed Jafry to its board of directors. - 8/3/18 -
7 important takeaways from the FDA's medical device safety action plan
The FDA released a medical device safety action plan to protect patients and promote public health. - 8/3/18
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