exGraft ePTFE Vascular Graft, exGraft Carbon ePTFE Vascular Graft— 510(k) K202471

Name: FDA 510(k) clearance K202471
Creator: U.S. Food and Drug Administration
Published: 2020-12-11

Substantially Equivalent

Peca Labs

FDA 510(k) clearance K202471 for exGraft ePTFE Vascular Graft, exGraft Carbon ePTFE Vascular Graft, Substantially Equivalent on 2020-12-11. Applicant: Peca Labs. Device class: 2.

Clearance details

Applicant: Peca Labs
Product code: Code DSY
Device class: Class 2
Regulation: 21 CFR 870.3450
Advisory panel: Cardiovascular
Date received: 2020-08-28
Decision date: 2020-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pittsburgh, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DSY

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K252445 — Fusion Bioline Vascular Graft2026-04-27
K252277 — Spiral Laminar Flow Vascular Arteriovenous Graft (AV0645)2025-10-20
K241550 — Gelweave Vascular Prostheses2025-02-27
K241070 — Gelsoft Plus Vascular Prostheses2024-11-15
K231972 — Advanta VXT Vascular Graft, Flixene Vascular Graft2024-03-28

More clearances from Peca Labs

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K221628 — exGraft, exGraft Carbon2022-08-04
K183613 — exGraft, exGraft Carbon2019-04-22
K180957 — exGraft, exGraft Carbon ePTFE Vascular Grafts2018-08-21

Adverse events under product code DSY

product code DSY

Death: 29
Injury: 694
Total: 723

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.