Last synced on 13 June 2025 at 11:06 pm

PIEZOTOME CUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172137
510(k) Type
Traditional
Applicant
Satelec - Acteon Group
Country
France
FDA Decision
Substantially Equivalent
Decision Date
5/3/2018
Days to Decision
290 days
Submission Type
Summary

PIEZOTOME CUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172137
510(k) Type
Traditional
Applicant
Satelec - Acteon Group
Country
France
FDA Decision
Substantially Equivalent
Decision Date
5/3/2018
Days to Decision
290 days
Submission Type
Summary