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DualX Lumbar Intervertebral Body Fusion Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192434
510(k) Type
Special
Applicant
Amplify Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2019
Days to Decision
40 days
Submission Type
Summary

DualX Lumbar Intervertebral Body Fusion Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192434
510(k) Type
Special
Applicant
Amplify Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2019
Days to Decision
40 days
Submission Type
Summary