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LOQTEQ Distal Lateral Femur Plate 4.5 System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210043
510(k) Type
Traditional
Applicant
AAP Implantate AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/3/2021
Days to Decision
55 days
Submission Type
Summary

LOQTEQ Distal Lateral Femur Plate 4.5 System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210043
510(k) Type
Traditional
Applicant
AAP Implantate AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/3/2021
Days to Decision
55 days
Submission Type
Summary