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ET Hybrid Abutment

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162390
510(k) Type
Traditional
Applicant
HIOSSEN INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2017
Days to Decision
157 days
Submission Type
Summary

ET Hybrid Abutment

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162390
510(k) Type
Traditional
Applicant
HIOSSEN INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2017
Days to Decision
157 days
Submission Type
Summary