Last synced on 14 November 2025 at 11:06 pm

BD Trek Powered Bone Biopsy System

Page Type
Cleared 510(K)
510(k) Number
K213896
510(k) Type
Traditional
Applicant
Bard Peripheral Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/2022
Days to Decision
106 days
Submission Type
Summary

BD Trek Powered Bone Biopsy System

Page Type
Cleared 510(K)
510(k) Number
K213896
510(k) Type
Traditional
Applicant
Bard Peripheral Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/2022
Days to Decision
106 days
Submission Type
Summary