# K122216: Reliance Anterior Cervical Plate System

- Pathway: 510(k) (Traditional)
- Applicant: Reliance Medical Systems, LLC
- Decided: Sep 5, 2012 after 42 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
Longest line of descent: 7 generations back to K922087 (1992). 40 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 44 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030866: Synthes Anterior CSLP System, Synthes (Usa) (2003) Summary page 1.
- K945700: Synthes (Usa) Anterior Cervical Vertebrae Plate System, Synthes (Usa) (1995) Summary page 1.
- K042798: C-Tek C-Trun Anterior Cervical Plate System, Interpore Cross Intl. (2004) Summary page 1.
- K070891: Altiva Classic Acp System, Altiva Corp. (2007) Summary page 1.
- K100614: Hallmark Anterior Cervcial Plate System, Hallmark Five-Level Cervical Plates, Blackstone Medical, Inc. (2010) Summary page 1.
- K083663: PACP, Pioneer Surgical Technology (2009) Summary page 1.
- K052292: Spider Cervical Plating (SCP) System, X-Spine Systems, Inc. (2005) Summary page 1.
- K953720: Aesculap Caspar Plate & Screw System for Anterior Cervical Fusion, Aesculap, Inc. (1995) Summary page 1.

## Most influential descendants
- K140742: Reliance Anterior Cervical Plate (2014), 2 descendants of its own
- K221572: VyPlate Anterior Cervical Plate System (2022), 1 descendant of its own
- K260697: VyPlate™ Anterior Cervical Plate System (2026), 0 descendants of its own

## Indications for use
The Reliance Anterior Cervical Plate System is indicated for stabilization of the anterior cervical spine from C2 to C7 employing unicortical screw fixation at the anterior face of the vertebral bodies. Specific clinical indications for anterior plating include: * instability caused by trauma or fracture; * instability associated with correction of cervical lordosis and kyphosis deformity; * instability associated with pseudoarthosis as a result of previously failed cervical spine surgery; * instability associated with major reconstructive surgery for primary tumors oirmetastatic malignant tumors of the cervical spine; * instability associated with single or multiple level corpectomy in advanced degenerative disk disease (defined as discogenic pain with degeneration of the disc confirmed by history and iradiographic studies), spinal canal stenosis and cervical myelopathy. This device is not approved for screw attachment or fixation to the posterior elements (pedicles) of the cervical, thoracic, or lumbar spine.

Source page: https://510kreport.com/device/K122216
Methodology: https://510kreport.com/methodology