# K061721: Pedi-Spider Strap

- Pathway: 510(k) (Traditional)
- Applicant: Emergency Products and Research
- Decided: Aug 17, 2006 after 59 days
- Product code: NZD (Stretcher, Patient Restraint)
- Device class: 1
- Regulation: 21 CFR 880.6900
- 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) Pedo Cush Pedo Cuddle: named in the summary without a submission number

## Indications for use
The Pedi-Spider strap is designed for securing a pediatric patient to a long spine board, by the use of a checker board series of straps that are placed over the patient and secure to the back board with Velcro hook and loop closures on each side of the back board. The device should be used on children from 10 to 100 pounds and 12 to 55 inches in height. The Pedi-Spider strap is designed for securing a pediatric patient to a long spine board. This would be used in the event of an injury, or suspected injury to the spinal area of a pediatric patient. The purpose of this device is to immobilize the patient while being stabilized at the scene of an emergency and during the transport of the patient to a treating medical facility. The device works by having a series of straps that are placed over the body of the patient and secured to the sides of the backboard with loop and hook closures. This series of straps are connected on each side and in the middle of the device to provide stability and extra rigidity.

Source page: https://510kreport.com/device/K061721
Methodology: https://510kreport.com/methodology