WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO— 510(k) K874740
Substantially Equivalent for Some IndicationsDow Corning Wright
FDA 510(k) clearance K874740 for WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO, Substantially Equivalent for Some Indications on 1987-12-18. Applicant: Dow Corning Wright.
Clearance details
- Applicant
- Dow Corning Wright
- Product code
- Code JDG
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Arlington, TN, US
Adverse events under product code JDG
product code JDG- Injury
- 804
- Malfunction
- 3,242
- Total
- 4,046
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.