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HG II FIXTURE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K090237
510(k) Type
Traditional
Applicant
HIOSSEN INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2009
Days to Decision
74 days
Submission Type
Summary

HG II FIXTURE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K090237
510(k) Type
Traditional
Applicant
HIOSSEN INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2009
Days to Decision
74 days
Submission Type
Summary