Last synced on 25 January 2026 at 3:41 am

LOQTEQ® VA Distal Tibia Plate System: LOQTEQ® VA Distal Medial Tibia Plate 3.5; LOQTEQ® VA Distal Anterolateral Tibia Plate 3.5; LOQTEQ® VA Distal Fibula Plate 2.7/3.5

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161747
510(k) Type
Traditional
Applicant
Aap Implantate AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
11/22/2016
Days to Decision
151 days
Submission Type
Summary

LOQTEQ® VA Distal Tibia Plate System: LOQTEQ® VA Distal Medial Tibia Plate 3.5; LOQTEQ® VA Distal Anterolateral Tibia Plate 3.5; LOQTEQ® VA Distal Fibula Plate 2.7/3.5

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161747
510(k) Type
Traditional
Applicant
Aap Implantate AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
11/22/2016
Days to Decision
151 days
Submission Type
Summary