BIOMET ANTERIOR LUMBAR PLATE— 510(k) K082187

Substantially Equivalent

Ebi, L.P.

FDA 510(k) clearance K082187 for BIOMET ANTERIOR LUMBAR PLATE, Substantially Equivalent on 2008-11-13. Applicant: Ebi, L.P..

Clearance details

Applicant: Ebi, L.P.
Product code: Code KWQ
Advisory panel: Orthopedic
Date received: 2008-08-04
Decision date: 2008-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Parsippany, NJ, US

Download summary PDF View on FDA.gov ↗

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.