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REPROCESSED EXTERNAL FIXATION ACCESSORIES

Page Type
Cleared 510(K)
510(k) Number
K081342
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2008
Days to Decision
92 days
Submission Type
Summary

REPROCESSED EXTERNAL FIXATION ACCESSORIES

Page Type
Cleared 510(K)
510(k) Number
K081342
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2008
Days to Decision
92 days
Submission Type
Summary