# K962238: Select Shoulder Keeled All-Poly Glenoids

- Pathway: 510(k) (Traditional)
- Applicant: Intermedics Orthopedics
- Decided: Aug 9, 1996 after 59 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
No predicates in its family tree.
236 later devices descend from it; 1 cites it directly.
1 of 237 devices in its family (counting itself) has 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) Orthomet/3M Modular Neer II Shoulder System: named in the summary without a submission number
- (no number) Zimmer Fenlin Total Shoulder: named in the summary without a submission number
- (no number) Smith & Nephew Richards Cofield Shoulder: named in the summary without a submission number
- (no number) Kirschner/Biomet Modular Shoulder: named in the summary without a submission number
- (no number) Biomet Bio-Modular Total Shoulder: named in the summary without a submission number
- (no number) Depuy Global Total Shoulder System: named in the summary without a submission number

## Most influential descendants
- K982981: New Zimmer Shoulder System (1998), 235 descendants of its own
- K041549: Zimmer Trabecular Metal Humeral Stem (2004), 218 descendants of its own
- K052906: Zimmer Trabecular Metal Reverse Shoulder System (2005), 216 descendants of its own
- K060704: Zimmer Trabecular Metal Reverse Shoulder System, Sizes 8MM and 10MM (2006), 207 descendants of its own
- K063569: Equinoxe Reverse Shoulder System (2007), 190 descendants of its own

Source page: https://510kreport.com/device/K962238
Methodology: https://510kreport.com/methodology