EBI VERTEBROPLASTY SYSTEMS— 510(k) K060148

Substantially Equivalent

Ebi, L.P.

FDA 510(k) clearance K060148 for EBI VERTEBROPLASTY SYSTEMS, Substantially Equivalent on 2006-03-13. Applicant: Ebi, L.P..

Clearance details

Applicant: Ebi, L.P.
Product code: Code NDN
Advisory panel: Orthopedic
Date received: 2006-01-19
Decision date: 2006-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Parsippany, NJ, US

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Adverse events under product code NDN

product code NDN

Death: 24
Injury: 407
Malfunction: 1,975
Total: 2,406

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.