CCG CERCLAGE SYSTEM— 510(k) K932024
Substantially Equivalent for Some IndicationsEncore Orthopedics, Inc.
FDA 510(k) clearance K932024 for CCG CERCLAGE SYSTEM, Substantially Equivalent for Some Indications on 1995-02-14. Applicant: Encore Orthopedics, Inc..
Clearance details
- Applicant
- Encore Orthopedics, Inc.
- Product code
- Code JDQ
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Austin, TX, US
Adverse events under product code JDQ
product code JDQ- Death
- 9
- Injury
- 330
- Total
- 339
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.