# FDA 510(k) cleared: Catalyft PL Expandable Interbody System

> fda · VERIFIED · 2026-07-17

Applicant: Medtronic Sofamor Danek USA, Inc. · Substantially Equivalent

- Company: Medtronic Sofamor Danek USA, Inc.
- Sector: medical devices
- Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K253011

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.