Stelkast, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stelkast, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Provident II Hip Stem, GENFlex2 Total Knee System - Ultra-Congruent CR Tibial Insert
3
Total
3
Cleared
0
Denied
Stelkast, Inc. has 3 FDA 510(k) cleared medical devices. Based in Mcmurray, US.
Historical record: 3 cleared submissions from 2016 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Stelkast, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Musculoskeletal Clinical Regulatory Advisors and Musculoskeletal Clinical Regulatory Advisers, LLC.
FDA 510(k) Regulatory Record - Stelkast, Inc.
3 devices