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Hive™ Stand-alone Anterior Lumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K200541
510(k) Type
Traditional
Applicant
HD LifeSciences LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/2020
Days to Decision
56 days
Submission Type
Summary

Hive™ Stand-alone Anterior Lumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K200541
510(k) Type
Traditional
Applicant
HD LifeSciences LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/2020
Days to Decision
56 days
Submission Type
Summary