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Implant Planning Software

Page Type
Cleared 510(K)
510(k) Number
K173965
510(k) Type
Traditional
Applicant
Inteware Co. Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/26/2018
Days to Decision
301 days
Submission Type
Statement

Implant Planning Software

Page Type
Cleared 510(K)
510(k) Number
K173965
510(k) Type
Traditional
Applicant
Inteware Co. Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/26/2018
Days to Decision
301 days
Submission Type
Statement