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FDA feedback accelerates Monogram's 510(k) submission plans

EditorBrando Bricchi
Published 05/01/2024, 01:20 PM
MGRM
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AUSTIN, TX - Monogram Orthopaedics Inc. (NASDAQ:MGRM), an AI-driven robotics company specializing in orthopedic surgery, announced it is on track to accelerate its 510(k) submission to the U.S. Food and Drug Administration (FDA) for its mBôs™ Total Knee Arthroplasty (TKA) System. Following recent communications with the FDA, the company received positive feedback on April 19, 2024, regarding its pre-submission request and subsequent teleconference on April 24, 2024. The FDA's response supports a least burdensome approach to clinical data acquisition, which Monogram believes will aid in a successful submission.

The company's proposed clinical trial, set to involve approximately 100 knee surgeries on a non-U.S. population across three sites, should be sufficient to evaluate the safety and effectiveness of the mBôs™ TKA System. This strategy could save the company significant costs and time, estimated at $1.5M for the trial. Monogram has adjusted its system design to lessen the likelihood of the FDA requesting additional clinical data, with verification and validation testing expected to be largely complete in the first half of 2024.

Monogram's CEO, Ben Sexson, expressed confidence in the thorough testing and FDA feedback, anticipating the submission in the second half of 2024. Dave McGurl, Vice President of Regulatory Affairs at MCRA, a Contract Research Organization supporting Monogram, echoed this sentiment, highlighting the company's commitment to patient safety and regulatory compliance.

The company's upcoming milestones for 2024 include completing system verification and validation, submitting the 510(k) application, and commencing international clinical trials. Monogram's long-term goal is to enable patient-optimized orthopedic implants at scale by integrating 3D printing and robotics with advanced imaging.

Monogram Orthopaedics has not yet made 510(k) submissions or obtained clearances for its robotic products and cannot predict the timing or guarantee success in obtaining FDA approval. The information in this article is based on a press release statement.

InvestingPro Insights

As Monogram Orthopaedics Inc. (NASDAQ:MGRM) strides toward its FDA submission for the mBôs™ Total Knee Arthroplasty System, investors and industry watchers are keeping a keen eye on the company's financial health and market performance. According to recent data from InvestingPro, Monogram Orthopaedics holds a market capitalization of $65.32 million. Despite its innovative approach in the medical technology space, the company's financial metrics indicate challenges, with a negative P/E ratio of -4.75 for the last twelve months as of Q4 2023, underscoring the company's current lack of profitability.

InvestingPro Tips suggest that while analysts anticipate sales growth in the current year, they do not expect the company to be profitable within this timeframe. Additionally, Monogram's stock has experienced a significant downturn, with a one-year price total return of -82.43% as of the latest data. This volatility in the stock price reflects the high-risk nature often associated with early-stage medical technology companies.

On a more positive note, Monogram Orthopaedics holds more cash than debt on its balance sheet, which could provide a cushion as it navigates the regulatory pathway and works towards commercializing its TKA System. This financial stability is further reinforced by the fact that the company's liquid assets exceed its short-term obligations, an indicator of short-term financial health.

For those considering an investment in Monogram Orthopaedics or seeking more detailed analysis, InvestingPro offers a wealth of additional insights, with 10 more InvestingPro Tips available to subscribers. To access these insights and enhance your investment strategy, use coupon code PRONEWS24 for an additional 10% off a yearly or biyearly Pro and Pro+ subscription.

This article was generated with the support of AI and reviewed by an editor. For more information see our T&C.

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