THE ZIMMER TMT TRABECULAR METAL VERTEBRAL BODY REPLACEMENT SYSTEM— 510(k) K052950

Substantially Equivalent

Zimmer Trabecular

FDA 510(k) clearance K052950 for THE ZIMMER TMT TRABECULAR METAL VERTEBRAL BODY REPLACEMENT SYSTEM, Substantially Equivalent on 2005-11-16. Applicant: Zimmer Trabecular.

Clearance details

Applicant: Zimmer Trabecular
Product code: Code MQP
Advisory panel: Orthopedic
Date received: 2005-10-20
Decision date: 2005-11-16
Decision: Substantially Equivalent
Clearance type: Special
Location: Allendale, NJ, US

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Adverse events under product code MQP

product code MQP

Injury: 372
Malfunction: 519
Total: 891

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.