# K992344: Osteonics Accp System Line Extension

- Pathway: 510(k) (Special)
- Applicant: Howmedica Osteonics Corp.
- Decided: Jul 30, 1999 after 16 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; 2 cite 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) Osteonics® ACCP System: 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 the use of the Osteonics® ACCP System are as follows: e degenerative disc disease (neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies). e decompression of the spinal cord following total or partial cervical vertebrectomy e trauma (fractures) e tumors e pseudarthrosis ¢ failed previous fusions

Source page: https://510kreport.com/device/K992344
Methodology: https://510kreport.com/methodology