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STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063584
510(k) Type
Traditional
Applicant
REGENERATION TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2007
Days to Decision
159 days
Submission Type
Summary

STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063584
510(k) Type
Traditional
Applicant
REGENERATION TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2007
Days to Decision
159 days
Submission Type
Summary