Talos® Lumbar (HA) PEEK IBF Devices— 510(k) K170395

Substantially Equivalent

Meditech Spine, LLC

FDA 510(k) clearance K170395 for Talos® Lumbar (HA) PEEK IBF Devices, Substantially Equivalent on 2017-06-02. Applicant: Meditech Spine, LLC.

Clearance details

Applicant: Meditech Spine, LLC
Product code: Code MAX
Advisory panel: Orthopedic
Date received: 2017-02-08
Decision date: 2017-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Atlanta, GA, 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.