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EXACTECH EQUINOX SUPERIOR/POSTERIOR AUGMENT REVERSE SHOULDER GLENOID BASEPLATE - LEFT & RIGHT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131575
510(k) Type
Special
Applicant
EXACTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/2013
Days to Decision
33 days
Submission Type
Summary

EXACTECH EQUINOX SUPERIOR/POSTERIOR AUGMENT REVERSE SHOULDER GLENOID BASEPLATE - LEFT & RIGHT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131575
510(k) Type
Special
Applicant
EXACTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/2013
Days to Decision
33 days
Submission Type
Summary