Last synced on 25 January 2026 at 3:41 am

ENDOFUSE INTRA-OSSEOUS FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102324
510(k) Type
Traditional
Applicant
Wrightmedicaltechnologyinc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2011
Days to Decision
260 days
Submission Type
Summary

ENDOFUSE INTRA-OSSEOUS FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102324
510(k) Type
Traditional
Applicant
Wrightmedicaltechnologyinc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2011
Days to Decision
260 days
Submission Type
Summary