# K070836: Exiclip Excs-M

- Pathway: 510(k) (Traditional)
- Applicant: Clevex, Inc.
- Decided: Apr 20, 2007 after 24 days
- Product code: MJG (Device, Percutaneous, Biopsy)
- Device class: 1
- Regulation: 21 CFR 878.4800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Shoney Scientific Disposable Punch Biopsy: named in the summary without a submission number
- (no number) AutoClip® Applier; AutoClip® Wound Clip (Device: Skin Clip w/ Applicator): named in the summary without a submission number

## Indications for use
The ExiClipTM EXCS-M is intended to provide a biopsy specimen and/or without biopsy under clinical discretion, remove skin lesions less than 6mm in diameter where simultaneous wound closure is desired.

Source page: https://510kreport.com/device/K070836
Methodology: https://510kreport.com/methodology