PRO-LINK CERVICAL SPACER SYSTEM— 510(k) K121151

Substantially Equivalent

Life Spine, Inc.

FDA 510(k) clearance K121151 for PRO-LINK CERVICAL SPACER SYSTEM, Substantially Equivalent on 2012-11-16. Applicant: Life Spine, Inc..

Clearance details

Applicant: Life Spine, Inc.
Product code: Code OVE
Advisory panel: Orthopedic
Date received: 2012-04-16
Decision date: 2012-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hoffman Estates, IL, US

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Adverse events under product code OVE

product code OVE

Injury: 293
Malfunction: 710
Total: 1,003

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.