Zavation Posterior LEIF— 510(k) K142392

Substantially Equivalent

Zavation, LLC

FDA 510(k) clearance K142392 for Zavation Posterior LEIF, Substantially Equivalent on 2015-04-29. Applicant: Zavation, LLC.

Clearance details

Applicant: Zavation, LLC
Product code: Code MAX
Advisory panel: Orthopedic
Date received: 2014-08-27
Decision date: 2015-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Flowood, MS, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MAX

product code MAX

Death: 13
Injury: 1,305
Malfunction: 2,885
Total: 4,203

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.