# K971307: Amsco Surgical Table

- Pathway: 510(k) (Traditional)
- Applicant: STERIS Corporation
- Decided: Jun 27, 1997 after 80 days
- Product code: FQO (Table, Operating-Room, Ac-Powered)
- Device class: 1
- Regulation: 21 CFR 878.4960
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
12 later devices descend from it; 1 cites it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K090136: Steris Cmax XLT Surgical Table (2009), 11 descendants of its own
- K112109: The Kinegraph Vma Software, the Motion Normalizer Patient Handling and Data Collection Device (2011), 10 descendants of its own
- K130743: The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.0; the Motion Normalizer Patient Handling and Data Coll (2013), 9 descendants of its own
- K133875: The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.2, the Motion Normalizer Patient Handling and Data (2014), 8 descendants of its own
- K172327: VMA™ System version 3.0 (2017), 7 descendants of its own

## Indications for use
The AMSCO® Surgical Table is a mobile, electro-hydraulically operated general surgical table that provides flexible articulation and image amplification of the surgical patient.

Source page: https://510kreport.com/device/K971307
Methodology: https://510kreport.com/methodology