SPINAL POSITIONING FRAME— 510(k) K922371
Substantially EquivalentRhino Mfg.
FDA 510(k) clearance K922371 for SPINAL POSITIONING FRAME, Substantially Equivalent on 1992-06-04. Applicant: Rhino Mfg..
Clearance details
- Applicant
- Rhino Mfg.
- Product code
- Code FQO
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rancho Cordova, CA, US
Adverse events under product code FQO
product code FQO- Death
- 6
- Injury
- 145
- Malfunction
- 685
- Total
- 836
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.