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EQUINOXE UHMWPE 12* POSTERIOR AUGMENT PEGGED GLENOID, SMALL / MEDIUM / LARGE / EXTRA-LARGE, LEFT / RIGHT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111379
510(k) Type
Special
Applicant
EXACTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/2011
Days to Decision
22 days
Submission Type
Summary

EQUINOXE UHMWPE 12* POSTERIOR AUGMENT PEGGED GLENOID, SMALL / MEDIUM / LARGE / EXTRA-LARGE, LEFT / RIGHT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111379
510(k) Type
Special
Applicant
EXACTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/2011
Days to Decision
22 days
Submission Type
Summary