FRONTIER ANTERIOR SCOLIOSIS SYSTEM— 510(k) K012916

Substantially Equivalent

Depuy Acromed, Inc.

FDA 510(k) clearance K012916 for FRONTIER ANTERIOR SCOLIOSIS SYSTEM, Substantially Equivalent on 2001-11-27. Applicant: Depuy Acromed, Inc..

Clearance details

Applicant: Depuy Acromed, Inc.
Product code: Code KWQ
Advisory panel: Orthopedic
Date received: 2001-08-30
Decision date: 2001-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

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Adverse events under product code KWQ

product code KWQ

Death: 8
Injury: 1,212
Malfunction: 1,233
Total: 2,453

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.