DEPUY CAS KNEE INSTRUMENTATION— 510(k) K043223
Substantially EquivalentDePuy Orthopaedics, Inc.
FDA 510(k) clearance K043223 for DEPUY CAS KNEE INSTRUMENTATION, Substantially Equivalent on 2005-03-04. Applicant: DePuy Orthopaedics, Inc.. Device class: 2.
Clearance details
- Applicant
- DePuy Orthopaedics, Inc.
- Product code
- Code HAW
- Device class
- Class 2
- Regulation
- 21 CFR 882.4560
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Warsaw, IN, US
Recent devices under product code HAW
view allMore clearances from DePuy Orthopaedics, Inc.
view allAdverse events under product code HAW
product code HAW- Death
- 52
- Injury
- 1,083
- Malfunction
- 17,300
- Total
- 18,435
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 →
Recalls naming K043223
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K043223.
Data sourced from openFDA. This site is unofficial and independent of the FDA.