# K963413: Multiple Limb Holders

- Pathway: 510(k) (Traditional)
- Applicant: J. T. Posey Co.
- Decided: Nov 14, 1996 after 76 days
- Product code: FMQ (Restraint, Protective)
- Device class: 1
- Regulation: 21 CFR 880.6760
- Recalls of this device: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K110377: Protective Restraint (2011), 0 descendants of its own

## Recalls of this device
- Sep 8, 2008 · Not classified · Z-0934-2009: The recall was initiated after an investigation conducted by the Posey Company determined that a patient may be able to catch the belt on a stationary object (wall, pipe, etc.) and use their body forc
- Jul 25, 2008 · Not classified · Z-0286-2009: Failure to restrain: This recall was initiated after a complaint was received by the firm regarding a Posey 2217SL unit indicating that a patient was able to pull the rivet or washer through the synth

## Indications for use
These products are intended to limit limb movement or finger movement in a hospital bed or gurney.

Source page: https://510kreport.com/device/K963413
Methodology: https://510kreport.com/methodology