Adaptix Interbody System with Titan nanoLOCK Surface Technology— 510(k) K250669
Substantially EquivalentMedtronic Sofamor Danek USA, Inc.
FDA 510(k) clearance K250669 for Adaptix Interbody System with Titan nanoLOCK Surface Technology, Substantially Equivalent on 2025-04-22. Applicant: Medtronic Sofamor Danek USA, Inc..
Clearance details
- Applicant
- Medtronic Sofamor Danek USA, Inc.
- Product code
- Code MAX
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Memphis, TN, US
Adverse events under product code MAX
product code MAX- Death
- 13
- Injury
- 1,305
- Malfunction
- 2,885
- Total
- 4,203
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.