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Additive Orthopaedics® Announces New Patient Educational Website www TotalTalusReplacement com

Share this article Share this article LITTLE SILVER, N.J., March 10, 2021 /PRNewswire/ Additive Orthopaedics, LLC., the leader in 3D printed orthopaedic foot and ankle devices, announces the launch of a new educational website focused on the Patient Specific Talus Spacer. The website, www.TotalTalusReplacement.com, contains information about avascular necrosis ( AVN ) for patients and surgeons. (PRNewsfoto/Additive Orthopaedics, LLC.) Additive Orthopaedics received an approval order in February 2021 from the U.S. Food and Drug Administration ( FDA ) for its Humanitarian Device Exemption application for the Patient Specific Talus Spacer for treatment of AVN of the talus. The approval order made the Additive Orthopaedics Patient Specific Talus Spacer the first and only patient specific total talus replacement implant approved by the FDA for use in the United States.

Carissa kennisonAdditive orthopaedicsPatient specific talus spacerகரிசா கெண்ணிசோன்நோயாளி குறிப்பிட்ட தாலஸ் ஸ்பேசர்

Additive Orthopaedics® Announces New Patient Educational Website www TotalTalusReplacement com

Additive Orthopaedics® Announces New Patient Educational Website www TotalTalusReplacement com
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Carissa kennisonAdditive orthopaedicsPatient specific talus spacerகரிசா கெண்ணிசோன்நோயாளி குறிப்பிட்ட தாலஸ் ஸ்பேசர்

FDA approves 3D-printed ankle implant for humanitarian use

FDA approves 3D-printed ankle implant for humanitarian use
medtechdive.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from medtechdive.com Daily Mail and Mail on Sunday newspapers.

Dive briefPatient specific talus spacerAdditive orthopaedicsடைவ் சுருக்கமானநோயாளி குறிப்பிட்ட தாலஸ் ஸ்பேசர்

FDA approves novel 3D-printed talus implant for humanitarian use

FDA approves novel 3D-printed talus implant for humanitarian use Today, the U.S. Food and Drug Administration approved the Patient Specific Talus Spacer 3D-printed talus implant for humanitarian use. The Patient Specific Talus Spacer is the first in the world and first-of-its-kind implant to replace the talus the bone in the ankle joint that connects the leg and the foot for the treatment of avascular necrosis (AVN) of the ankle joint, a serious and progressive condition that causes the death of bone tissue stemming from a lack of blood supply to the area. The implant provides a joint-sparing alternative to other surgical interventions commonly used in late-stage AVN that may disable motion of the ankle joint.

Emily hendersonRadiological health office of orthopedic devicesDrug administrationPatient specific talus spacer to additive orthopaedicsPatient specific talus spacerRaquel peatRadiological healthHumanitarian use deviceAdditive orthopaedicsAvascular necrosisஎமிலி ஹென்டர்சன்கதிரியக்கவியல் ஆரோக்கியம் அலுவலகம் ஆஃப் எலும்பியல் சாதனங்கள்நோயாளி குறிப்பிட்ட தாலஸ் ஸ்பேசர் க்கு எலும்பியல்நோயாளி குறிப்பிட்ட தாலஸ் ஸ்பேசர்ரகெல் கரிகதிரியக்கவியல் ஆரோக்கியம்

Additive Orthopaedics® Announces FDA Approval of Patient Specific Talus Spacer, First Approved in the U S

(MENAFN - PR Newswire) LITTLE SILVER, N.J., Feb. 17, 2021 /PRNewswire/ Â Additive Orthopaedics, LLC., announced today it has received an approval order from the U.S. Food and Drug Administration ( FDA ) for its Humanitarian Device Exemption ( HDE ) application for the Patient Specific Talus Spacer for treatment of avascular necrosis of the talus. The approval order makes the Additive Orthopaedics Patient Specific Talus Spacer the first and only patient specific total talus replacement implant approved by the FDA for use in the United States. Continue Reading (PRNewsfoto/Additive Orthopaedics, LLC.) The Patient Specific Talus Spacer is indicated for Avascular Necrosis ( AVN ) of the ankle joint. Under the HDE, the Patient Specific Talus Spacer will be made available as a humanitarian use device, defined by the FDA as one intended to benefit patients in the treatment or diagnosis of a disease or condition that affects or is manifested in not more than 8,000 individuals in the

United statesGreg kowalczykpresidentGreg kowalczykDrug administrationAdditive orthopaedicsPrnewsfoto additive orthopaedicsHumanitarian device exemptionPatient specific talus spacerContinue readingAvascular necrosisPr newswireWhat time is itFree fire vs pubgLook likeHuawei p30 lite vs samsung a50ஒன்றுபட்டது மாநிலங்களில்