Biopsy needles
Finesse
by Bard Peripheral Vascular, Inc.
An invasive tubular surgical instrument designed to be connected to a biopsy gun handpiece (not included) for the automatic extraction of a small tissue sample from an anatomical structure (a biopsy), while causing minimal surrounding tissue damage, for tissue pathological examination/testing. It is a percutaneously-inserted needle with a side-notch cutter at the distal end which when activated causes a sharp, sliding cannula to slice a segment of tissue. It is typically used to obtain samples of soft tissue from the kidneys, prostate, pancreas, liver, and breast, often performed under image guidance. This is a single-use device.
Finesse models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| F01BLU | — | Not stated | Available |
FDA clearances
- 510(k) K103359 December 2010
Procedures that use biopsy needles
Frequently asked questions
What is Finesse used for?
An invasive tubular surgical instrument designed to be connected to a biopsy gun handpiece (not included) for the automatic extraction of a small tissue sample from an anatomical structure (a biopsy), while causing minimal surrounding tissue damage, for tissue pathological examination/testing. It is a percutaneously-inserted needle with a side-notch cutter at the distal end which when activated causes a sharp, sliding cannula to slice a segment of tissue. It is typically used to obtain samples of soft tissue from the kidneys, prostate, pancreas, liver, and breast, often performed under image guidance. This is a single-use device.
Who makes Finesse?
Finesse is made by Bard Peripheral Vascular, Inc.. It is listed under biopsy needles and systems in our device library.
What sizes does Finesse come in?
The FDA device database does not list sizes for Finesse. Check the instructions for use or ask a Bard Peripheral Vascular, Inc. representative.
Is Finesse MRI safe?
The FDA device database entry for Finesse does not state its MRI safety status. Check the labeling before MRI.
Is Finesse FDA cleared?
Finesse is covered by FDA submission K103359.
How do I contact a Bard Peripheral Vascular, Inc. sales representative?
Bard Peripheral Vascular, Inc. has not listed representatives on LA Vascular yet. Visit the Bard Peripheral Vascular, Inc. company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.