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L300 PLUS SYSTEM (RIGHT, LEFT), L300 PLUS SYSTEM UPGRADE KIT (RIGHT, LEFT)

Page Type
Cleared 510(K)
510(k) Number
K103343
510(k) Type
Traditional
Applicant
BIONESS INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2011
Days to Decision
165 days
Submission Type
Summary

L300 PLUS SYSTEM (RIGHT, LEFT), L300 PLUS SYSTEM UPGRADE KIT (RIGHT, LEFT)

Page Type
Cleared 510(K)
510(k) Number
K103343
510(k) Type
Traditional
Applicant
BIONESS INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2011
Days to Decision
165 days
Submission Type
Summary