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ATLANTIS ABUTMENT AND ATLANTIS ABUTMENT SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981858
510(k) Type
Traditional
Applicant
Atlantis Components, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1999
Days to Decision
299 days
Submission Type
Summary

ATLANTIS ABUTMENT AND ATLANTIS ABUTMENT SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981858
510(k) Type
Traditional
Applicant
Atlantis Components, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1999
Days to Decision
299 days
Submission Type
Summary