POPMESH— 510(k) K053424
Substantially EquivalentCaldera Medical, Inc.
FDA 510(k) clearance K053424 for POPMESH, Substantially Equivalent on 2006-02-22. Applicant: Caldera Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Caldera Medical, Inc.
- Product code
- Code FTL
- Device class
- Class 2
- Regulation
- 21 CFR 878.3300
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Agoura Hills, CA, US
Recent devices under product code FTL
view allMore clearances from Caldera Medical, Inc.
view allAdverse events under product code FTL
product code FTL- Death
- 317
- Injury
- 66,072
- Malfunction
- 1,273
- Other
- 3
- Total
- 67,665
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.