REVCON (TM) Screw System— 510(k) K223392
Substantially EquivalentVoom Medical Devices, Inc.
FDA 510(k) clearance K223392 for REVCON (TM) Screw System, Substantially Equivalent on 2023-02-28. Applicant: Voom Medical Devices, Inc..
Clearance details
- Applicant
- Voom Medical Devices, Inc.
- Product code
- Code HWC
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York City, NY, US
Adverse events under product code HWC
product code HWC- Death
- 20
- Injury
- 15,910
- Malfunction
- 8,192
- Other
- 1
- Total
- 24,123
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.