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REPROCESSED EXTERNAL FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K083636
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2009
Days to Decision
83 days
Submission Type
Summary

REPROCESSED EXTERNAL FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K083636
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2009
Days to Decision
83 days
Submission Type
Summary