Last synced on 25 January 2026 at 3:41 am

STAGEONE SELECT CEMENT SPACER MOLDS FOR TEMPORARY HIP REPLACEMENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080979
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2008
Days to Decision
207 days
Submission Type
Summary

STAGEONE SELECT CEMENT SPACER MOLDS FOR TEMPORARY HIP REPLACEMENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080979
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2008
Days to Decision
207 days
Submission Type
Summary