Caprolon— 510(k) K181320
Substantially EquivalentResorba Medical GmbH
FDA 510(k) clearance K181320 for Caprolon, Substantially Equivalent on 2018-09-18. Applicant: Resorba Medical GmbH. Device class: 2.
Clearance details
- Applicant
- Resorba Medical GmbH
- Product code
- Code GAM
- Device class
- Class 2
- Regulation
- 21 CFR 878.4493
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Nuremberg, DE
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More clearances from Resorba Medical GmbH
view allAdverse events under product code GAM
product code GAM- Death
- 45
- Injury
- 5,711
- Malfunction
- 30,744
- Other
- 4
- Total
- 36,504
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.