SMITH & NEPHEW MODULAR FEMORAL (HEMI) HEAD— 510(k) K062408
Substantially EquivalentSmith & Nephew, Inc.
FDA 510(k) clearance K062408 for SMITH & NEPHEW MODULAR FEMORAL (HEMI) HEAD, Substantially Equivalent on 2006-09-12. Applicant: Smith & Nephew, Inc.. Device class: 2.
Clearance details
- Applicant
- Smith & Nephew, Inc.
- Product code
- Code KWL
- Device class
- Class 2
- Regulation
- 21 CFR 888.3360
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Memphis, TN, US
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Adverse events under product code KWL
product code KWL- Injury
- 523
- Total
- 523
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.