Exactech Australia Pty Ltd
Regulatory activities for this sponsor.
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Sponsor content
129 result(s) found, displaying 1 to 10
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Exactech Australia Pty Ltd - Equinoxe Small Reverse Shoulder Humeral Liner - Reverse shoulder prosthesis cup.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Exactech Australia Pty Ltd - Equinoxe Small Reverse Shoulder Superior/Posterior Augment Glenoid Plate - Reverse shoulder prosthesis base plate.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Exactech Australia Pty Ltd - Equinoxe Small Reverse Shoulder Constrained Humeral Liner - Reverse shoulder prosthesis cup.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Exactech Australia Pty Ltd - Equinoxe Small Reverse Shoulder Superior Augment Glenoid Plate 10 degree - Reverse shoulder prosthesis base plate.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Exactech Australia Pty Ltd - Equinoxe Small Reverse Shoulder Standard Glenoid Plate - Reverse shoulder prosthesis base plate.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Exactech Australia Pty Ltd - Equinoxe Small Reverse Shoulder Glenoid Plate, +10mm Extended Cage Peg - Reverse shoulder prosthesis base plate.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Exactech Australia Pty Ltd - Equinoxe Small Reverse Shoulder Posterior Augment Glenoid Plate 8 degree - Reverse shoulder prosthesis base plate.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Exactech Australia Pty Ltd - Equinoxe Small Reverse Glenospheres - Reverse shoulder prosthesis head.
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Cancellation or suspensionCancellation of the entry as the sponsor did not provide information to substantiate compliance with the Essential Principles, the sponsor failed to comply with a condition to which inclusion of the kind of device in the ARTG was subject under s.41FN(3)(a).
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Cancellation or suspensionCancellation of the entry as the sponsor did not provide information to substantiate compliance with the Essential Principles, the sponsor failed to comply with a condition to which inclusion of the kind of device in the ARTG was subject under s.41FN(3)(a).