NNA

Biopsy Device, Percutaneous, Reprocessed

Product code

NNA

Device name

Biopsy Device, Percutaneous, Reprocessed

Device class

Class 1

21 CFR

21 CFR 878.4800

Medical specialty

General, Plastic Surgery

Marketing pathway

510(K)

Flag

Third-party review eligible

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).

Definition text from the FDA device classification database (U.S. federal government work, public domain).