Last synced on 20 December 2024 at 11:05 pm

Solo+ Tympanostomy Tube Device (TTD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232702
510(k) Type
Traditional
Applicant
AventaMed DAC
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
5/20/2024
Days to Decision
258 days
Submission Type
Summary

Solo+ Tympanostomy Tube Device (TTD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232702
510(k) Type
Traditional
Applicant
AventaMed DAC
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
5/20/2024
Days to Decision
258 days
Submission Type
Summary