Last synced on 30 May 2025 at 11:05 pm

APTUS Cannulated Compression Screws, APTUS headed Cannulated Compression Screws, APTUS K-Wire System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202589
510(k) Type
Traditional
Applicant
Medartis AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
11/6/2020
Days to Decision
59 days
Submission Type
Summary

APTUS Cannulated Compression Screws, APTUS headed Cannulated Compression Screws, APTUS K-Wire System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202589
510(k) Type
Traditional
Applicant
Medartis AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
11/6/2020
Days to Decision
59 days
Submission Type
Summary