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Home/Large Joints and Extremities/Continuous Compression Extremity Device Cleared by FDA
Large Joints and Extremities

Continuous Compression Extremity Device Cleared by FDA

March 12, 2018 1 min read Premium comments

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Continuous Compression Extremity Device Cleared by FDA
Source: Wikimedia Commons and Anatomy & Physiology, Connexions Web site. http://cnx.org/content/col11496/1.6/, Jun 19, 2013.
#fdaSecondary#Pantherorthopedics#jointfixation

San Jose-based Panther Orthopedics, Inc.’s, flexible extremity joint fixation device has been cleared by the FDA for sale in the U.S.

The Puma System is indicated for syndesmosis fixation, hallux valgus reconstruction, and tarsometatarsal fixation.

While the FDA action is a clearance, meaning the device was essentially equivalent to a previously approved device, the company claims the Puma system “represents a revolutionary advancement in the treatment of orthopedic injuries by allowing normal anatomical motion of the joint while maintaining continuous compression.”

According to a March 7, 2018 company announcement by Kathy Stecco, M.D., company co-founder and CEO, the system was designed to “solve the problems experienced with the use of stiff metal screws which serve as stress risers and prohibit normal physiological joint motion and with flexible fixation devices that creep and therefore lose compression.”

Kenneth Hunt, M.D., associate professor and chief of foot and ankle, University of Colorado Department of Orthopaedics, said the system is unique in that it “provides stabilization of the joint with a consistent force, allowing rotational flexibility without displacement or creep.”

The system allows for a 2.8mm pilot hole that preserves bone tissue and comes in one size for a simple, customized approach that can be trimmed to the specific anatomy to provide stable dynamic fixation of the joint, said the company.

The start-up company announced a Series A investment by Taiwan-based medical device company, Medeon Biodesign, Inc., about a year ago.

At the time, the company pointed to a need for better fixation products for both trauma and sports medicine in fracture fixation and joint stabilization applications that were still under served.

“Current options for fixation include cortical screw and suture button flexible fixation devices. However, many limitations associated with currently marketed products are not being addressed,” said Stecco. “We have developed an innovative platform for dynamic extremity fixation, which we believe will provide continuous compression during the healing period while still allowing micromotion. The intuitive design of our solutions is easy to use and intended to eliminate the need for most second surgery removal, providing significant benefits for both the patients and the entire healthcare system.”

React:

Discussion

14
DS
Dr. Sarah MitchellOrthopedic Surgeon · Mayo Clinic

This is a fascinating development. In my practice we've seen similar outcomes with the revised protocol. The key differentiator seems to be patient selection criteria. Has anyone else noticed the correlation with BMI thresholds?

8
JT
James Thornton, MDSpine Fellow · HSS

Great point. I'd push back slightly on the conclusion, the sample size in the cited study is too small to draw population-level inferences. That said, the directional signal is compelling and worth a larger RCT.

5
RP
R. PatelSports Medicine · Stanford

We implemented a similar approach last year. Early results are promising but we're still gathering 12-month follow-up data. Happy to share our protocol if anyone is interested.

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