# K102709: Peak Plasmablade Plus Tissue Dissection Device

- Pathway: 510(k) (Special)
- Applicant: Peak Surgical, Inc.
- Decided: Dec 17, 2010 after 88 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 13 generations back to K936109 (1994). 79 ancestors in all.
No later device cites it as a predicate yet.
0 of 80 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K093695: Peak Plasmablade 3.OS Tissue Dissection Device, Peak Surgical, Inc. (2010) Summary page 1.
- K083415: Peak Plasmablade Tna Tonsil and Adenoid Tissue Dissection Device, Peak Surgical, Inc. (2009) Summary page 1.
- K780976: Single Use Ball Electrode, Aspen Laboratories, Inc. (1978) Summary page 1.

## Indications for use
The PEAK PlasmaBlade®o PLUS Tissue Dissection Device is indicated for cutting and coagulation of soft tissue during General, Plastic and Reconstructive (including but not limited to skin incisions and development of skin flaps), ENT, Gynecologic, Orthopaedic, Arthroscopic, Spinal and Neurological surgical procedures.

Source page: https://510kreport.com/device/K102709
Methodology: https://510kreport.com/methodology