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REPROCESSED EXTERNAL FIXATION ACCESSORIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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