Tele: 561.316.3330
Breaking Medical Device News

Monday, September 27, 2021
HomeDextera Surgical Inc.Dextera Surgical’s MicroCutter 5/80 Featured in Preclinical Laparoscopic Nephrectomy Study at SAGES Annual Meeting

Dextera Surgical’s MicroCutter 5/80 Featured in Preclinical Laparoscopic Nephrectomy Study at SAGES Annual Meeting

Dextera Surgical Inc. (Nasdaq:DXTR), manufacturer of the smallest-profile and most maneuverable articulating surgical stapling platform on the market for minimally invasive surgery, today announced that leading surgeon Juan-Carlos Verdeja, M.D., presented a poster highlighting the MicroCutter Stapler as a procedure enabling technology in laparoscopic nephrectomy for kidney removal in an animal model.

“The results of the preclinical study show that the MicroCutter had equivalent hemostasis to a conventional three-row surgical stapler in a preclinical study of laparoscopic nephrectomy procedures,” said Dr. Verdeja, associate professor of surgery and director, minimally invasive surgery at Florida International University College of Medicine and chief of general surgery division at Baptist Health Medical Group. “With more surgeons using minimally invasive approaches for nephrectomy and removing donor kidneys, we showed that the slim jaws of the MicroCutter create a small footprint on the vessels, increasing the length of the retained vascular stump by up to 1.6mm, which is especially critical in donor nephrectomy transplant cases.”

In the poster, Dr. Verdeja presented results from 13 firings of the MicroCutter (5 millimeters in diameter) and 14 firings of a conventional three-row endostapler (12 millimeters in diameter). The study evaluated hemostasis (stopping of blood flow) and staple line quality when firing on the renal artery and renal vein as well as the ureter. Importantly, these firings demonstrate the MicroCutter’s performance on blood vessels with systemic pressures that come directly off the aorta and vena cava. After firing the stapler on these vessels, hypertension was induced for three minutes to further challenge hemostasis at the staple line.

The data demonstrate that there was no bleeding at any of the staple lines from either the MicroCutter or the conventional endostapler at initial firing or upon induction of hypertension. There were no adverse events associated with either device. The data were presented at the Society of American Gastrointestinal and Endoscopic Surgeons Meeting (SAGES) in Houston, Texas, beginning Thursday, March 23, 2017 at 10:00 a.m. local time. [Poster # P421] Full study results are expected to be published later this year in a peer-reviewed publication.

“Dr. Verdeja’s data confirm the excellent hemostasis results seen in previous studies of the MicroCutter,” commented Liam Burns, vice president of worldwide sales and marketing. “Additionally, this study demonstrates that the MicroCutter, due to its small footprint and 80 degrees of articulation, may enable less invasive surgical approaches in urology such as donor nephrectomy transplant procedures, extending the applications of our surgical stapler beyond thoracic, pediatric, and general surgery.”

 

Medical Device News Magazinehttps://infomeddnews.com
Medical Device News Magazine is a division of PTM Healthcare Marketing, Inc. Pauline T. Mayer is the managing editor.

Stay Connected

spot_img

Don't Miss

ProSomnus® Sleep Technologies Adds John E. Remmers, MD, to Leadership Team

Dr. John E. Remmers will provide expert medical and strategic guidance on a range of initiatives, including research and development, regulatory clearances, company strategy, medical education, and clinical investigations.

Nanox to Announce Zebra Medical Vision Secures 8th 510K FDA Clearance for its Coronary Artery Calcium (CAC) Solution as Part of Its Population Health Offering

On August 10th, 2021 Nanox announced that it had entered into an acquisition agreement via merger with Zebra Medical Vision LTD.

Christopher Joyce Joins Miach Orthopaedics as VP & CFO

Christopher Joyce has joined as vice president and chief financial officer, and Kevin Sidow has been appointed to the company’s board of directors.

NGMedical GmbH Receives FDA Clearance for Its AM Titanium Lumbar Interbody BEE® PLIF

The BEE® PLIF cage has been created to benefit from additive manufacturing features. The purposefully designed honeycomb endplate design reduces the risk of subsidence, while allowing fusion.

Recombinant Technologies is Raising Capital to Roll Out a Game Changing Alzheimer’s Treatment

Recombinant Technologies is focused on treating the root cause of Alzheimer's Disease delivering a huge improvement in the quality of life of those afflicted.

Tyber Medical Reaches Agreement to Acquire CatapultMD

Once the acquisition is complete, Tyber Medical will own and operate a combined 100,000-square feet of manufacturing space between its Pennsylvania headquarters and Florida-based facilities.

Kleiner Device Labs Receives FDA Market Clearance for KG2 Surge Flow-Thru Interbody System

The system maximizes total bone graft delivery volume, better distributes graft bilaterally into the intervertebral disc space, and streamlines the implant delivery, positioning, and grafting process for TLIF and PLIF spinal fusion procedures.

Matthew Cranfill New ExtriCARE USA Director Of Clinical Services

"Matt's impressive experience and skillset easily made him our top pick," said Peter Mason, President of ExtriCARE USA.

By using this website you agree to accept Medical Device News Magazine Privacy Policy