AXTi Titanium Stand-Alone ALIF System— 510(k) K182139

Substantially Equivalent

Innovasis, Inc.

FDA 510(k) clearance K182139 for AXTi Titanium Stand-Alone ALIF System, Substantially Equivalent on 2019-06-21. Applicant: Innovasis, Inc..

Clearance details

Applicant: Innovasis, Inc.
Product code: Code OVD
Advisory panel: Orthopedic
Date received: 2018-08-07
Decision date: 2019-06-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code OVD

product code OVD

Death: 5
Injury: 495
Total: 500

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.