Last synced on 30 September 2022 at 11:05 pm

ATLANTIS ABUTMENT FOR BIOHORIZON IMPLANTS, ATLANTIS GEMINI ABUTMENT FOR BIOHORIZON IMPLANTS, ATLANTIS GEMINI + ABUTMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073258
510(k) Type
Traditional
Applicant
ATLANTIS COMPONENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2008
Days to Decision
86 days
Submission Type
Summary

ATLANTIS ABUTMENT FOR BIOHORIZON IMPLANTS, ATLANTIS GEMINI ABUTMENT FOR BIOHORIZON IMPLANTS, ATLANTIS GEMINI + ABUTMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073258
510(k) Type
Traditional
Applicant
ATLANTIS COMPONENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2008
Days to Decision
86 days
Submission Type
Summary