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K3PRO Konus Additional Abutments and Implants

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160581
510(k) Type
Traditional
Applicant
Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/24/2017
Days to Decision
388 days
Submission Type
Summary

K3PRO Konus Additional Abutments and Implants

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160581
510(k) Type
Traditional
Applicant
Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/24/2017
Days to Decision
388 days
Submission Type
Summary