# K150730: Zimmer PSI Shoulder System

- Pathway: 510(k) (Traditional)
- Applicant: Zimmer
- Decided: Jun 16, 2015 after 88 days
- Product code: KWT (Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented)
- Device class: 2
- Regulation: 21 CFR 888.3650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K911686 (1991). 42 ancestors in all.
11 later devices descend from it; 1 cites it directly.
0 of 54 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131129: Cas Psi Shoulder, Zimmer Cas (2013) Summary page 4.

## Most influential descendants
- K190595: Signature ONE System (2019), 10 descendants of its own
- K192074: Signature ONE System (2019), 9 descendants of its own
- K200615: Signature ONE System (2020), 8 descendants of its own
- K212560: Signature™ ONE System (2021), 7 descendants of its own
- K222007: Arthrex Virtual Implant Positioning (VIP) System (2023), 3 descendants of its own

## Indications for use
The Zimmer® PSI Shoulder is indicated, based on patient-specific radiological images with identifiable placement anatomical landmarks, to assist in pre-operative planning and/or intra-operative guiding of surgical instruments for shoulder replacement surgical procedures on patients not precluded from being radiologically scanned. The Zimmer® PSI Shoulder is to be used with the glenoid components of the following shoulder implant systems in accordance with their indications and contraindications: Zimmer® Bigliani/Flatow® Complete Shoulder Solution, Zimmer® Trabecular Metal™ Glenoid, and Zimmer® Trabecular Metal™ Reverse Shoulder. The Zimmer® PSI Shoulder instrument guides and bone model are intended for single use only.

Source page: https://510kreport.com/device/K150730
Methodology: https://510kreport.com/methodology