KENSEY NASH BONE VOID FILLER XC— 510(k) K120141

Name: FDA 510(k) clearance K120141
Creator: U.S. Food and Drug Administration
Published: 2012-05-04

Unknown

Kensey Nash Cororation

FDA 510(k) clearance K120141 for KENSEY NASH BONE VOID FILLER XC, Unknown on 2012-05-04. Applicant: Kensey Nash Cororation. Device class: 2.

Clearance details

Applicant: Kensey Nash Cororation
Product code: Code MQV
Device class: Class 2
Regulation: 21 CFR 888.3045
Advisory panel: Orthopedic
Date received: 2012-01-18
Decision date: 2012-05-04
Decision: Unknown
Clearance type: Traditional
Location: Exton, PA, US

Download summary PDF View on FDA.gov ↗

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K253524 — Adaptos®Fuse Bone Graft2026-02-17

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.