STALIF MIDLINE— 510(k) K101301

Name: FDA 510(k) clearance K101301
Creator: U.S. Food and Drug Administration
Published: 2010-09-24

Substantially Equivalent

Centinel Spine

FDA 510(k) clearance K101301 for STALIF MIDLINE, Substantially Equivalent on 2010-09-24. Applicant: Centinel Spine. Device class: 2.

Clearance details

Applicant: Centinel Spine
Product code: Code MAX
Device class: Class 2
Regulation: 21 CFR 888.3080
Advisory panel: Orthopedic
Date received: 2010-05-10
Decision date: 2010-09-24
Decision: Substantially Equivalent
Clearance type: Special
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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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.