Last synced on 14 November 2025 at 11:06 pm

PIEZOTOME

Page Type
Cleared 510(K)
510(k) Number
K060275
510(k) Type
Traditional
Applicant
SATELEC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2006
Days to Decision
90 days
Submission Type
Summary

PIEZOTOME

Page Type
Cleared 510(K)
510(k) Number
K060275
510(k) Type
Traditional
Applicant
SATELEC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2006
Days to Decision
90 days
Submission Type
Summary