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REPROCESSED EXTERNAL FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K051957
510(k) Type
Traditional
Applicant
STERILEMED INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2005
Days to Decision
68 days
Submission Type
Summary

REPROCESSED EXTERNAL FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K051957
510(k) Type
Traditional
Applicant
STERILEMED INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2005
Days to Decision
68 days
Submission Type
Summary