PremiPatch PTFE Pledget— 510(k) K151865

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K151865 for PremiPatch PTFE Pledget, Substantially Equivalent on 2015-10-27. Applicant: Aesculap, Inc..

Clearance details

Applicant: Aesculap, Inc.
Product code: Code DXZ
Advisory panel: Cardiovascular
Date received: 2015-07-08
Decision date: 2015-10-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Center Valley, PA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DXZ

product code DXZ

Death: 19
Injury: 265
Total: 284

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.