OSMA Fellows

masthead Fellows

Honoring your legacy in orthopaedics

Becoming an OSMA Fellow is a prestigious distinction reserved for individuals who have significantly shaped the organization’s path and success. This exclusive membership recognizes your pivotal contributions and invites continued involvement in advancing the field of orthopaedics.

What to expect as an OSMA Fellow

As an OSMA Fellow, you will enjoy a variety of opportunities and benefits that empower you to continue making an impact in the orthopaedic field:

Access to exclusive resources

OSMA Fellows have privileged access to:

img s3 Access to exclusive resources
img s3 Leadership mentorship Participation Opportunities

Leadership, Mentorship and Participation Opportunities

OSMA Fellows are invited to take on leadership and mentorship roles, including:

Travel reimbursement

OSMA recognizes your valuable contributions and provides travel reimbursement under certain conditions:

img s3 Travel reimbursement

Honoring distinguished leaders who have shaped orthopedic regulatory excellence

The OSMA Fellows program would like to recognize these exceptional professionals who have made significant and lasting contributions to the orthopedic medical device industry and to OSMA throughout their distinguished careers.

OSMA Fellow Pics Ed Circle

Ed Chin

OSMA Fellow Pics Sharon CIrcle

Sharon Starowicz

OSMA Fellow Pics ROdney CIrcle

Rodney Parker

Member qualifications

Becoming an OSMA Fellow is a distinguished honor, and the selection process is rigorous to maintain the prestige of this recognition.

Join the legacy of OSMA Fellows

If you have made significant contributions to the OSMA organization and are ready to be recognized for your efforts, we invite you to join the esteemed ranks of OSMA Fellows.

To express your interest in becoming an OSMA Fellow or to nominate a colleague, please fill out the form. Our team will review your submission and contact you with further details.

OSMA Fellow Nominee Information
OSMA Fellow Pics Ed Circle

Ed Chin


Twenty-seven years in orthopedic regulatory affairs at Medtronic established Ed Chin as a respected leader in navigating complex regulatory pathways. His expertise in managing multiple PMA submissions and FDA advisory committee processes became particularly valuable as the regulatory landscape evolved, especially with the introduction of EU MDR requirements that reshaped global clinical trial strategies.

Ed's OSMA legacy centers on two landmark regulatory achievements: leading the cervical screw down-classification initiative and championing the amendment to the Federal Food, Drug, and Cosmetic Act regarding custom devices. These accomplishments required exceptional consensus-building skills and deep regulatory knowledge.

Throughout nearly two decades with OSMA, Ed valued his Board service alongside distinguished industry leaders. The collaborative relationships he built with both industry peers and FDA colleagues through OSMA exemplify the organization's mission of advancing orthopedic regulatory science through partnership and shared expertise.

OSMA Fellow Pics Sharon CIrcle

Sharon Starowicz


With over three decades in orthopedic regulatory affairs, Sharon Starowicz has been a driving force in shaping industry-regulator relationships. She began her career at FDA as a Biomedical Engineer and Scientific Reviewer in the Orthopedics group before moving to Johnson & Johnson, where she advanced to lead regulatory, clinical and quality operations for major business initiatives.

Sharon's seven-year tenure as OSMA President transformed the organization into a trusted partner with FDA. Her leadership helped establish OSMA as a key communication channel for regulatory requirements and industry coordination efforts. She later served as Industry Representative to the FDA Orthopedic Devices Panel, cementing her role as a bridge between the two communities.

Having participated in OSMA for over 30 years, Sharon witnessed its evolution from intimate ten-person gatherings to robust meetings with strong FDA participation. Her notable achievements include spearheading successful device classification efforts and representing OSMA at industry forums, always working to advance the field through collaboration and education.

OSMA Fellow Pics ROdney CIrcle

Rodney Parker


Rod Parker dedicated 28 years to orthopedic regulatory affairs at Stryker Instruments, where he developed a uniquely comprehensive approach as Manager of Regulatory Affairs for the Instruments Division. His department oversaw not only traditional regulatory functions but also specialized disciplines of sterilization, biocompatibility, and instrument processing—creating one of the most interesting and diverse regulatory departments in the industry.

Rod's expertise extended beyond Stryker through his active participation as a sitting member of four ISO and AAMI standards committees, bringing cutting-edge regulatory insights to the OSMA membership over 20 years. Beginning his OSMA journey in 1996 when meetings drew just nine attendees, Rod witnessed the organization's remarkable growth, attending an impressive 85 quarterly meetings throughout his career.

His most significant OSMA contribution came as chair of the endotoxin issue with FDA in 2016, leading a complex negotiation that resulted in additional testing requirements rather than mandatory labeling for orthopedic implants. Rod considers this challenging outcome a proud achievement in representing both OSMA and the broader industry, demonstrating his ability to navigate the evolving approaches of FDA and international regulatory agencies.