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Straumann BLX Implant System

Page Type
Cleared 510(K)
510(k) Number
K173961
510(k) Type
Traditional
Applicant
Institut Straumann AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
6/5/2018
Days to Decision
159 days
Submission Type
Summary

Straumann BLX Implant System

Page Type
Cleared 510(K)
510(k) Number
K173961
510(k) Type
Traditional
Applicant
Institut Straumann AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
6/5/2018
Days to Decision
159 days
Submission Type
Summary