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ATR 3000, ATR 2000, IMPLANT-PRO

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991401
510(k) Type
Traditional
Applicant
Advanced Technology Research (A.T.R.) S.R.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/1999
Days to Decision
237 days
Submission Type
Summary

ATR 3000, ATR 2000, IMPLANT-PRO

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991401
510(k) Type
Traditional
Applicant
Advanced Technology Research (A.T.R.) S.R.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/1999
Days to Decision
237 days
Submission Type
Summary