Last synced on 30 May 2025 at 11:05 pm

EQUINOXE REVERSE SHOULDER SYSTEM FRACTURE HUMERAL ADAPTER TRAY AND LOCKING SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073688
510(k) Type
Special
Applicant
EXACTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/29/2008
Days to Decision
63 days
Submission Type
Summary

EQUINOXE REVERSE SHOULDER SYSTEM FRACTURE HUMERAL ADAPTER TRAY AND LOCKING SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073688
510(k) Type
Special
Applicant
EXACTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/29/2008
Days to Decision
63 days
Submission Type
Summary