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HD Lumbar Interbody System

Page Type
Cleared 510(K)
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)
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