Last synced on 25 January 2026 at 3:41 am

MODIFICATION TO DEPUY DELTA XTEND REVERSE SHOULDER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081620
510(k) Type
Special
Applicant
DePuy Orthopaedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2008
Days to Decision
21 days
Submission Type
Summary

MODIFICATION TO DEPUY DELTA XTEND REVERSE SHOULDER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081620
510(k) Type
Special
Applicant
DePuy Orthopaedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2008
Days to Decision
21 days
Submission Type
Summary