Last synced on 25 January 2026 at 3:41 am

LOQTEQ DISTAL DORSOLATERAL HUMERUS PLATE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132787
510(k) Type
Traditional
Applicant
Aap Implantate AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
12/24/2013
Days to Decision
109 days
Submission Type
Summary

LOQTEQ DISTAL DORSOLATERAL HUMERUS PLATE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132787
510(k) Type
Traditional
Applicant
Aap Implantate AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
12/24/2013
Days to Decision
109 days
Submission Type
Summary