Genesys Spine TiLock2 Spinal System— 510(k) K152039

Substantially Equivalent

Genesys Spine

FDA 510(k) clearance K152039 for Genesys Spine TiLock2 Spinal System, Substantially Equivalent on 2015-10-28. Applicant: Genesys Spine.

Clearance details

Applicant: Genesys Spine
Product code: Code NKB
Advisory panel: Orthopedic
Date received: 2015-07-22
Decision date: 2015-10-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Austin, Tx, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code NKB

product code NKB

Death: 27
Injury: 5,033
Malfunction: 4,140
Total: 9,200

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.