share_log

Monogram Technologies Receives FDA Response for MBôs TKA System

Monogram Technologies Receives FDA Response for MBôs TKA System

Monogram Technologies收到FDA對MBôs TKA系統的回應
Accesswire ·  10/03 06:00

Company to Conduct Clinical Trial to Produce Additional Information Within 180 Days

公司將進行臨床試驗,在180天內提供額外信息

AUSTIN, TX / ACCESSWIRE / October 2, 2024 / Monogram Technologies Inc. (NASDAQ:MGRM) ("Monogram" or the "Company"), an AI-driven robotics company focused on improving human health with an initial focus on orthopedic surgery, today announced that it has received an Additional Information Request ("AIR") from the U.S. Food and Drug Administration ("FDA") on September 30, 2024, regarding its 510(k) premarket filing submission for the Company's mBôs TKA System (the "Application").

德克薩斯州奧斯汀 / ACCESSWIRE / 2024年10月2日 / Monogram Technologies Inc.(納斯達克:MGRM)("Monogram"或"公司"),一家專注於改善人體健康的人工智能驅動機器人公司,最初專注於整形外科手術,今天宣佈,公司於2024年9月30日收到了美國食品藥品監督管理局("FDA")要求提供額外信息的通知("AIR"),涉及公司mBôs TKA系統的510(k)預市場申請提交("申請")。

The Application was submitted on July 19, 2024, and passed the initial FDA Administrative Review. The FDA informed the Company that the FDA placed the Application on hold pending a complete response to the AIR. The FDA has informed the Company that the Company has 180 days from the date of the AIR to provide a complete response to the AIR or the FDA will consider the Application withdrawn.

該申請於2024年7月19日提交,並通過了首次FDA行政審查。FDA通知公司,由於AIR的完整回覆尚未提供,FDA已將該申請暫停。FDA通知公司,公司從AIR的日期起有180天時間提供AIR的完整回覆,否則FDA將考慮撤回該申請。

"We believe this response provides more transparency for Monogram's path forward toward obtaining clearance and ultimately commercialization," said Ben Sexson, CEO of Monogram Technologies. "We feel the increased clarity regarding the potential suitability of Indian clinical data is de-risking. Having just closed our upsized and oversubscribed $13 million public offering, Monogram will continue to execute on our strategic objectives. With growing surgeon support and market interest, we continue to believe in our thesis for orthopedic robotics and the value proposition of our proposed active robotic system. The highest priority for the Company remains obtaining FDA clearance as quickly and economically as possible. Management believes the FDA feedback was comprehensive and provides a framework to execute."

"我們相信這一回應爲Monogram前進的道路提供了更多透明度,以獲得許可並最終實現商業化,"Monogram Technologies首席執行官本·塞克森(Ben Sexson)表示。"我們認爲有關印度臨床數據潛在適用性的清晰性增加了降低風險。剛剛結束我們超額認購的1300萬美元的公開發行後,Monogram將繼續執行我們的戰略目標。隨着持續增加的外科醫生支持和市場興趣,我們仍然相信我們對整形外科機器人和提議的主動機器人系統的價值主張論。公司的首要任務仍然是儘快和經濟地獲得FDA許可。管理層認爲FDA的反饋全面,並提供了執行框架。"

As the Company works to respond to the AIR, the Company, in parallel, will pursue a submission for its active modality with Outside the United States ("OUS") clinical data as it continues to work through the AIR for its semi-active system.

隨着公司努力回應AIR,在同一時間,公司將尋求使用海外臨床數據提交其主動模式,同時繼續通過半主動系統的AIR。

"The Company has committed considerable resources to cadaveric system demos this quarter. We feel the surgeon feedback and market interest is greatest for our hands-free, fully active system. We are increasingly confident such system could be a game-changing advancement for the industry. This response provides more transparency for Monogram's path forward toward obtaining clearance and ultimately commercialization," Mr. Sexson continued."

公司在本季度致力於屍體系統演示,我們認爲外科醫生的反饋和市場興趣對於我們的免提、全動態系統是最大的。我們越來越確信這樣的系統可能會成爲行業的一項改變性進展。Sexson先生繼續說:「這一回應爲Monogram向前邁進以獲得許可和最終商業化提供了更多透明度。」

Upcoming Milestones

即將到來的里程碑

  • Obtain regulatory clearance to conduct clinical trials in India with strategic partner Shalby Hospitals, with clearance expected in early Q1 2025.

  • Conduct OUS live-patient surgery trials and submit clinical trial data to FDA, with clinical trials expected to include 92 total knee replacement procedures with a 3 month clinical follow-up.

  • Seek to obtain clearance for the mBôs TKA System.

  • Continue exploring domestic relationships.

  • Continue expanding international relationships (the Company will be exhibiting at Arab Health in January 2025).

  • 與戰略合作伙伴Shalby Hospitals在印度獲得進行臨床試驗的監管許可,預計將在2025年第一季度早期獲得許可。

  • 進行海外病患手術試驗,並向FDA提交臨床試驗數據,預計臨床試驗將包括92例總膝關節置換手術,並進行爲期3個月的臨床隨訪。

  • 尋求獲得mBôs TKA系統的許可。

  • 繼續探索國內關係。

  • 繼續擴大國際關係(公司將在2025年1月參加「阿拉伯衛生展」)。

About Monogram Technologies Inc.

關於蒙納克科技公司

Monogram Technologies (NASDAQ: MGRM) is an AI-driven robotics company focused on improving human health, with an initial focus on orthopedic surgery. The Company is developing a product solution architecture to enable patient-optimized orthopedic implants at scale by combining 3D printing, advanced machine vision, AI and next-generation robotics.

Monogram Technologies(納斯達克:MGRM)是一家以人工智能驅動的機器人公司,專注於改善人類健康,首要關注點是整形外科手術。公司正在開發產品解決方案架構,通過結合3d打印、先進的機器視覺、人工智能和下一代機器人技術,實現規模化的患者定製整形植入物。

Monograms mBôs precision robotic surgical system is designed to autonomously execute optimized paths for high-precision insertion of its FDA-cleared mPress press-fit implants. The goal is well balanced better-fitting bone sparing knee replacements. The Company initially intends to produce and market robotic surgical equipment and related software, orthopedic implants, tissue ablation tools, navigation consumables, and other miscellaneous instrumentation necessary for reconstructive joint replacement procedures. Other clinical and commercial applications for the mBôs with mVision navigation are also being explored.

Monograms mBôs精密機器人手術系統旨在自主執行優化路徑,精確插入其獲得FDA認證的mPress插件。其目標是更好地平衡、適配的省骨膝關節置換。該公司最初的目標是生產和銷售機器人手術設備和相關軟件、骨科植入物、組織消融工具、導航耗材和其他必要的關節重建手術器械。mBôs與mVision導航的其他臨床和商業應用也正在探索中。

Monogram has obtained FDA clearance for mPress implants and applied for 510(k) clearance for its robotic products. The Company is required to obtain FDA clearance before it can market its products. Monogram cannot estimate the timing or assure the ability to obtain such clearances.

Monogram已獲得mPress植入物的FDA批准,並申請了510(k)適用於其機器人產品的批准。在公司營銷其產品之前,必須獲得FDA的批准。Monogram無法估計獲得批准的時間或保證獲得此類批准的能力。

The Company believes that its mBôs precision robotic surgical assistants, which combine AI and novel navigation methods (mVision), will enable more personalized knee implants for patients, resulting in well balanced better-fitting knee replacements with bone sparing implants. Monogram anticipates that there may be other clinical and commercial applications for its navigated mBôs precision robot and mVision navigation.

公司認爲,它的mBôs精密機器人手術助手,將結合人工智能和新穎的導航方法(mVision),爲患者提供更個性化的膝關節植入物,從而實現平衡更好,更貼合的關節置換,減少骨骼損耗。蒙納克預計其具有mVision導航的mBôs精密機器人和mVision導航可能有其他臨床和商業應用。

To learn more, visit monogramtechnologies.com.

想要了解更多,請訪問monogramtechnologies.com。

Forward-Looking Statements

前瞻性聲明

This press release may contain "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Statements other than statements of historical facts included in this press release may constitute forward-looking statements and are not guarantees of future performance or results and involve a number of risks and uncertainties. For example, the Company's statement regarding the Company's proposed use of net proceeds is a forward-looking statement. Forward-looking statements, other than statements of historical fact, are highly likely to be affected by other unknowable future events and conditions, including elements of the future that are or are not under our control, and that the Company may or may not have considered; accordingly, such statements cannot be guarantees or assurances of any aspect of future performance. Actual developments and results are highly likely to vary materially from any forward-looking statements as a result of a number of factors, including those described in the prospectus and the Company's other filings with the SEC. The Company undertakes no duty to update any forward-looking statement made herein. All forward-looking statements speak only as of the date of this press release.

本新聞稿可能包含《1995年私人證券訴訟改革法案》中的「前瞻性聲明」。包括在本新聞稿中的除歷史事實陳述以外的其他陳述可能構成前瞻性陳述,不代表未來業績或結果的保證,並涉及多項風險和不確定性。例如,該公司有關擬議使用淨收益的聲明就是一項前瞻性聲明。前瞻性陳述,除了歷史事實陳述外,很可能受到其他無法預知的未來事件和條件的影響,包括我們控制或未控制的未來元素,以及該公司可能考慮或未考慮的因素;因此,這些陳述不能保證或保證未來業績的任何方面。由於多種因素的影響,實際發展和結果高度可能與任何前瞻性陳述有所不同,其中包括招股說明書和公司在SEC的其他備案中所述。該公司不承擔更新此處所述的任何前瞻性陳述的義務。所有前瞻性陳述僅作本新聞稿發出之日的陳述。

Investor Relations

投資者關係

Chris Tyson
Executive Vice President
MZ North America
Direct: 949-491-8235
MGRM@mzgroup.us

Chris Tyson
執行副總裁
MZ北美
直接撥打:949-491-8235
MGRM@mzgroup.us

Contact Information

聯繫信息

Chris Tyson
Executive Vice President
mgrm@mzgroup.us
949-491-8235

Chris Tyson
執行副總裁
mgrm@mzgroup.us
949-491-8235

SOURCE: Monogram Technologies Inc.

信息來源:蒙納克科技公司

譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
    搶先評論