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REPROCESSED EXTERNAL FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K081586
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2008
Days to Decision
74 days
Submission Type
Summary

REPROCESSED EXTERNAL FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K081586
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2008
Days to Decision
74 days
Submission Type
Summary