VISTA-S DEVICE MODEL 08/06-401-XXXXX, 08/06-402-XXXXXX— 510(k) K111983
Substantially EquivalentZimmer Trabecular Metal Technology
FDA 510(k) clearance K111983 for VISTA-S DEVICE MODEL 08/06-401-XXXXX, 08/06-402-XXXXXX, Substantially Equivalent on 2011-11-18. Applicant: Zimmer Trabecular Metal Technology.
Clearance details
- Applicant
- Zimmer Trabecular Metal Technology
- Product code
- Code ODP
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Parsippany, NJ, US
Adverse events under product code ODP
product code ODP- Injury
- 310
- Total
- 310
Source: openFDA MAUDE database, through . 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.