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GPS Angled Abutment

Page Type
Cleared 510(K)
510(k) Number
K153509
510(k) Type
Traditional
Applicant
IMPLANT DIRECT SYBRON MANUFACTURING LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2016
Days to Decision
263 days
Submission Type
Summary

GPS Angled Abutment

Page Type
Cleared 510(K)
510(k) Number
K153509
510(k) Type
Traditional
Applicant
IMPLANT DIRECT SYBRON MANUFACTURING LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2016
Days to Decision
263 days
Submission Type
Summary