SpeedBird Model SB38 Soft Tissue Biopsy Device +2 more— 510(k) K173316

Name: FDA 510(k) clearance K173316
Creator: U.S. Food and Drug Administration
Published: 2018-06-19

Substantially Equivalent

Transmed7, LLC

FDA 510(k) clearance K173316 for SpeedBird Model SB38 Soft Tissue Biopsy Device +2 more, Substantially Equivalent on 2018-06-19. Applicant: Transmed7, LLC. Device class: 2.

Clearance details

Device name as filed: SpeedBird Model SB38 Soft Tissue Biopsy Device; SpeedBird Model SBU Soft Tissue Biopsy Device; SpeedBird Model SBU99 Soft Tissue Biopsy Device
Applicant: Transmed7, LLC
Product code: Code KNW
Device class: Class 2
Regulation: 21 CFR 876.1075
Advisory panel: Gastroenterology, Urology
Date received: 2017-10-19
Decision date: 2018-06-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portola Valley, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KNW

product code KNW

Death: 9
Injury: 965
Malfunction: 10,444
Other: 3
Total: 11,421

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.