FDA Cleared
New Device
Pathway: 510K
Symmetrix PX Spinal System
Applicant:
Medtronic Sofamor Danek USA, Inc.
MDT
Statutory Profile
Legal Standard:
Substantial Equivalence (SE) to predicate (21 CFR 807)
Product Code:
MAX
Review Panel:
Orthopedic
21 CFR Regulation:
8
Review Velocity Metrics
Date Received:
2026-07-27
Decision Date:
2026-10-29
Total Review Duration:
94 calendar days (94 days)
Official FDA Research Backlinks
Direct links to primary official records hosted by the U.S. Food and Drug Administration CDRH databases:
Identified Contacts & Correspondents
Elizabeth Hamilton
Role: SUBMITTER_CONTACT
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