# K010811: Perc-D Spinewand

- Pathway: 510(k) (Traditional)
- Applicant: Arthrocare Corp.
- Decided: May 30, 2001 after 72 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
72 later devices descend from it; 5 cite it directly.
0 of 73 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K020621: Arthrocare Controller; Arthrocare Cable; Foot Control; Power Cord; Wands (2002), 33 descendants of its own
- K030954: Arthrocare Percd Spinewand (2003), 32 descendants of its own
- K032473: Dekompressor Percutaneous Discectomy Probe (2003), 28 descendants of its own
- K040338: Arthrocare Controller, Cable, Foot Control, Power Cord, Wands, Models H0970-02, H2000-04, H2000-05, H0970-06 (2004), 24 descendants of its own
- K071963: Modification to: Arthrocare Arthrowands (2007), 21 descendants of its own

Source page: https://510kreport.com/device/K010811
Methodology: https://510kreport.com/methodology