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RIGIDLOOP Titanium Button , RIGIDLOOP Cortical Fixation System XL Implant

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190774
510(k) Type
Traditional
Applicant
Medos International SARL
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
7/25/2019
Days to Decision
121 days
Submission Type
Summary

RIGIDLOOP Titanium Button , RIGIDLOOP Cortical Fixation System XL Implant

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190774
510(k) Type
Traditional
Applicant
Medos International SARL
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
7/25/2019
Days to Decision
121 days
Submission Type
Summary