Overview
Paige Cappelli primarily focuses on patent prosecution and patent litigation in the mechanical and medical device areas.
Paige graduated magna cum laude from Temple University Beasley School of Law. While attending Temple University, Paige served as President of the Intellectual Property Law Society. Prior to law school, Paige received her BS in Industrial Engineering from California Polytechnic State University, San Luis Obispo.
Paige worked as a summer associate at the firm in 2019 and joined the firm in 2021.
Clerk Experience
Judicial Intern for the Honorable Kenneth J. Powell, Jr., Philadelphia Court of Common Pleas
Education
- Temple University Beasley School of Law (J.D., 2020), Magna Cum Laude
- California Polytechnic State University - San Luis Obispo (CAL POLY) (B.S. Industrial Engineering, 2017), Cum Laude
News & Insights
Articles
Litigation Blog
Medical Device Blog
- ARPA-H Announces New Funding related to AI-Enabled Medical Tools
- Expect Future FDA Clarification on Machine Learning-Enabled Medical Devices
- FDA Releases Draft Guidances on 510(k) Submissions
- FDA Seeks $7.2 Billion Budget for 2024
- FDA to Collaborate With Veterans Group on Medical Device Innovation
- FDA Draft Guidance for Fostering Medical Device Improvement Using the Voluntary Improvement Program
- FDA Taking Steps to Prevent Future Medical Device Shortages
Aerospace Blog
Latest Updates and News
FAA Request for Information Related to a New Air Traffic Control Platform
The Federal Aviation Administration (FAA) issued a request for information (RFI) related to “a single, state-of-the art platform for air traffic control called the Common Automation Platform (CAP).” The CAP...
ARPA-H Announces New Funding related to AI-Enabled Medical Tools
The U.S. Advanced Research Projects Agency for Health (ARPA-H) announced new funding for a “program to help AI-enabled medical tools maintain peak performance.” The new funding is through the Performance and Reliability Evaluation for Continuous Modifications and Usability of Artificial Intelligence (PRECISE-AI) program.
Knobbe Martens Advises Vertos Medical, Inc. in Definitive Agreement To Be Acquired by Stryker
IRVINE, Calif., August 23, 2024 – Stryker, a global leader in medical technologies, announced today a definitive agreement to acquire Vertos Medical Inc., a privately held company providing a minimally...
Expect Future FDA Clarification on Machine Learning-Enabled Medical Devices
The inaugural AAMI/FDA neXus medical device standards conference was held February 20-23, 2024 in Washington DC. The conference was hosted by the Association for the Advancement of Medical Instrumentation (AAMI). Additional information regarding the conference can be found here.
FDA Releases Draft Guidances on 510(k) Submissions
On September 6, 2023, the U.S. Food & Drug Administration (FDA) released three draft guidance documents to provide updated recommendations on the 510(k) Program to “keep pace with the increasing complexity of rapidly evolving technology.” As stated on the FDA website: “[E]ach person who wants to market in the U.S., a Class I, II, and III device intended for human use, for which a Premarket Approval application (PMA) is not required, must submit a 510(k) to FDA unless” the device meets certain limited exemptions. A 510(k) submission provides, for the FDA’s review, safety and effectiveness data to show that a new device is substantially equivalent to a legally marketed predicate device.
FDA Seeks $7.2 Billion Budget for 2024
The FDA recently announced that it is seeking a budget of $7.2 Billion for 2024, part of which is intended for “Advancing Medical Product Availability.” The portion of the requested budget directed to advancing access to safe and effective medical products would be used toward various initiatives, three of which are highlighted in the FDA’s announcement.
