# K962486: Depuy Motech Anterior Compression Plate System

- Pathway: 510(k) (Traditional)
- Applicant: Depuy, Inc.
- Decided: Dec 27, 1996 after 184 days
- Product code: KWQ (Appliance, Fixation, Spinal Intervertebral Body)
- Device class: 2
- Regulation: 21 CFR 888.3060
- 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) Acromed AcroPlate Anterior Cervical System: named in the summary without a submission number
- (no number) Codman Anterior Cervical Plate System: named in the summary without a submission number
- (no number) Aesculap Cervical Plate System: named in the summary without a submission number

## Indications for use
The DePuy Motech PEAK™ Anterior Compression Plate System is intended for use in the treatment of anterior cervical spipe instability as a result of fractures, dislocations, subluxations, tumor, degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylosis or a previously failed cervical surgery.

Source page: https://510kreport.com/device/K962486
Methodology: https://510kreport.com/methodology