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Genesys Spine Binary Lumbar Plate System

Page Type
Cleared 510(K)
510(k) Number
K173885
510(k) Type
Traditional
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2018
Days to Decision
103 days
Submission Type
Summary

Genesys Spine Binary Lumbar Plate System

Page Type
Cleared 510(K)
510(k) Number
K173885
510(k) Type
Traditional
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2018
Days to Decision
103 days
Submission Type
Summary