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HD Lumbar Interbody System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170676
510(k) Type
Traditional
Applicant
Hd Lifesciences, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2017
Days to Decision
129 days
Submission Type
Summary

HD Lumbar Interbody System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170676
510(k) Type
Traditional
Applicant
Hd Lifesciences, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2017
Days to Decision
129 days
Submission Type
Summary