VARILIFT CERVICAL INTERBODY FUSION SYSTEM— 510(k) K111123

Substantially Equivalent

Wenzel Spine

FDA 510(k) clearance K111123 for VARILIFT CERVICAL INTERBODY FUSION SYSTEM, Substantially Equivalent on 2011-12-08. Applicant: Wenzel Spine.

Clearance details

Applicant: Wenzel Spine
Product code: Code ODP
Advisory panel: Orthopedic
Date received: 2011-04-21
Decision date: 2011-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Round Rock, TX, US

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Adverse events under product code ODP

product code ODP

Injury: 310
Total: 310

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.