BK241060 - Arthrex Thrombinator System
510(k) Number: 241060
Applicant: Arthrex, Inc.
Device Name: Arthrex Thrombinator System
Decision Date: 4/24/2024
On Oct. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. We are in the process of updating FDA.gov content to reflect these changes.
510(k) Number: 241060
Applicant: Arthrex, Inc.
Device Name: Arthrex Thrombinator System
Decision Date: 4/24/2024