# K963393: Mesh Vest Restraint with Sleeves Wrist/Ankle Restraint

- Pathway: 510(k) (Traditional)
- Applicant: Depuy, Inc.
- Decided: Oct 31, 1996 after 64 days
- Product code: FMQ (Restraint, Protective)
- Device class: 1
- Regulation: 21 CFR 880.6760
- Recalls of this device: none
- 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 its predicate without a number.
- (no number) J. T. Posey Co. Vest Restraint: named in the summary without a submission number
- (no number) J. T. Posey Co. Limb Holders: named in the summary without a submission number

## Most influential descendants
- K971742: Depuy Orthotech Heavy Duty Vest Restraint (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K963393
Methodology: https://510kreport.com/methodology