PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV— 510(k) K890182

Substantially Equivalent

Aesculap Instruments Corp.

FDA 510(k) clearance K890182 for PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV, Substantially Equivalent on 1990-02-28. Applicant: Aesculap Instruments Corp..

Clearance details

Applicant: Aesculap Instruments Corp.
Product code: Code DSY
Advisory panel: Cardiovascular
Date received: 1989-01-18
Decision date: 1990-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danville, CA, US

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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.