DR. HERZBERG DISPOSABLE EXTERNAL FIXATOR— 510(k) K890989
Substantially Equivalent for Some IndicationsOrigin Medsystems, Inc.
FDA 510(k) clearance K890989 for DR. HERZBERG DISPOSABLE EXTERNAL FIXATOR, Substantially Equivalent for Some Indications on 1990-04-05. Applicant: Origin Medsystems, Inc..
Clearance details
- Applicant
- Origin Medsystems, Inc.
- Product code
- Code KTT
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- San Mateo, CA, US
Adverse events under product code KTT
product code KTT- Death
- 11
- Injury
- 3,097
- Malfunction
- 1,261
- Total
- 4,369
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.