KENSEY NASH BONE VOID FILLER— 510(k) K060917

Substantially Equivalent

Kensey Nash Corporation

FDA 510(k) clearance K060917 for KENSEY NASH BONE VOID FILLER, Substantially Equivalent on 2006-09-22. Applicant: Kensey Nash Corporation.

Clearance details

Applicant: Kensey Nash Corporation
Product code: Code MQV
Advisory panel: Orthopedic
Date received: 2006-04-04
Decision date: 2006-09-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Exton, PA, US

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Adverse events under product code MQV

product code MQV

Death: 6
Injury: 435
Total: 441

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.