Last synced on 14 November 2025 at 11:06 pm

PLANMECA SOVEREIGN

Page Type
Cleared 510(K)
510(k) Number
K081699
510(k) Type
Traditional
Applicant
PLANMECA USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2008
Days to Decision
73 days
Submission Type
Summary

PLANMECA SOVEREIGN

Page Type
Cleared 510(K)
510(k) Number
K081699
510(k) Type
Traditional
Applicant
PLANMECA USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2008
Days to Decision
73 days
Submission Type
Summary