# K982798: Osteonics Anterior Cervical Compression Plating System

- Pathway: 510(k) (Traditional)
- Applicant: Osteonics Corp.
- Decided: Mar 25, 1999 after 227 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.
290 later devices descend from it; 1 cites it directly.
0 of 291 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) Synthes anterior cervical plates: named in the summary without a submission number

## Most influential descendants
- K000486: Abc Cervical Plating System (2000), 289 descendants of its own
- K050813: Abc 2 Screw (2005), 145 descendants of its own
- K133475: Struxxure Anterior Cervical Plate and Screws (2013), 132 descendants of its own
- K141376: Inertia Pedicle Screw System, Honour Spacer System, Facet Fixx, Struxxure Anterior Cervical Plate and Screws (2014), 106 descendants of its own
- K122910: Archon Anterior Cervical Plate Syste, (2012), 101 descendants of its own

## Indications for use
The indications for use of the Osteonics® ACCP System, in keeping with those of other legally marketed anterior cervical plates, are as follows. The Osteonics® ACCP System is intended for anterior intervertebral screw fixation of the cervical spine for the following indications: degenerative disc disease (neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies) deccompression of the spinal cord following total or partial cervical vertebrectomy trauma (fractures) tumors pseudarthrosis failed previous fusions

Source page: https://510kreport.com/device/K982798
Methodology: https://510kreport.com/methodology