510(k) K083186— AESCULAP HYDROLIFT VBR SYSTEM

Substantially Equivalent

Aesculap Implant System, Inc.

Clearance details

Applicant: Aesculap Implant System, Inc.
Product code: Code MQP
Advisory panel: Orthopedic
Date received: 2008-10-29
Decision date: 2010-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Center Valley, PA, US

Adverse events under product code MQP

product code MQP

Injury: 372
Malfunction: 519
Total: 891

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.