NLL
- Product code
- NLL
- Device name
- Staple, Implantable, Reprocessed
- Device class
- Class 2
- 21 CFR
- 21 CFR 878.4750
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 3
FDA classification definition
Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).
Official FDA classification page: NLL
Classification and pathway per current FDA publications. Data from openFDA (CC0).