# OsseoFit Stemless Shoulder System (K262955): 510(k) cleared for Zimmer, Inc.

**Predicate Speed & CAPA Advisory Opportunity Score:** 41/100

| Field | Value |
|---|---|
| Record | 510(k) clearance |
| 510(k) number | K262955 |
| Device | OsseoFit Stemless Shoulder System |
| Applicant | Zimmer, Inc. |
| Specialty / panel | Orthopedic |
| Product code | PKC |
| Device class | 2 |
| Clearance type | Special |
| Decision | Substantially Equivalent |
| Received | 2026-08-24 |
| Decision date | 2026-09-24 |
| Review time (days) | 31 |
| Third-party review | No |
| Applicant location | Warsaw, IN, US |

## Why this score
- Fast 31-day review: this device is a strong predicate for similar products.
- Special 510(k): a modification of an existing device.
- Posted 41 days ago.

Source: U.S. FDA openFDA (510(k) clearances and device enforcement reports) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K262955). Last refreshed: 2026-11-03T18:05:14.713Z.
Data from the FDA openFDA API, which may lag official FDA databases. Informational only; not regulatory or legal advice.