# K993181: Howmedica Osteonics Accp System Cortical Screws

- Pathway: 510(k) (Special)
- Applicant: Howmedica Osteonics Corp.
- Decided: Oct 22, 1999 after 29 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.
14 later devices descend from it; 1 cites it directly.
0 of 15 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) Howmedica Osteonics® ACCP System cortical bone screws: named in the summary without a submission number

## Most influential descendants
- K040017: Abc Caudal and Cranial Extension Plate (E-Plate) (2004), 13 descendants of its own
- K100243: Quintex Cervical Plating System (2010), 10 descendants of its own
- K141993: Nakoma Acp (2014), 8 descendants of its own
- K231766: Skyway Anterior Cervical Plate System (2023), 3 descendants of its own
- K243015: Skyway Anterior Cervical Plate System (2024), 2 descendants of its own

## Indications for use
The indications for the use of the Howmedica Osteonics® ACCP System are as follows: degenerative disc disease (neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies). decompression of the spinal cord following total or partial cervical vertebrectomy trauma (fractures) tumors pseudarthrosis failed previous fusions

Source page: https://510kreport.com/device/K993181
Methodology: https://510kreport.com/methodology