DUREPAIR DURA REGENERATION MATRIX— 510(k) K052211

Name: FDA 510(k) clearance K052211
Creator: U.S. Food and Drug Administration
Published: 2005-09-14

Substantially Equivalent

Medtronic Neurosurgery

FDA 510(k) clearance K052211 for DUREPAIR DURA REGENERATION MATRIX, Substantially Equivalent on 2005-09-14. Applicant: Medtronic Neurosurgery. Device class: 2.

Clearance details

Applicant: Medtronic Neurosurgery
Product code: Code GXQ
Device class: Class 2
Regulation: 21 CFR 882.5910
Advisory panel: Neurology
Date received: 2005-08-15
Decision date: 2005-09-14
Decision: Substantially Equivalent
Clearance type: Special
Location: Goleta, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GXQ

product code GXQ

Death: 11
Injury: 446
Other: 1
Total: 458

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.