Last synced on 14 November 2025 at 11:06 pm

FIXPINE II SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K100765
510(k) Type
Traditional
Applicant
DIO MEDICAL CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2010
Days to Decision
124 days
Submission Type
Summary

FIXPINE II SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K100765
510(k) Type
Traditional
Applicant
DIO MEDICAL CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2010
Days to Decision
124 days
Submission Type
Summary