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Biomet Australia Pty Ltd

Regulatory activities for this sponsor.

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Type

Cancellation by sponsor (76)
Cancellation or suspension (4)

Date

2015 (79)
2013 (1)

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Sponsor content

80 result(s) found, displaying 71 to 80

Biomet Australia Pty Ltd - Gauge, depth, surgical Cancelled under Section 41GL(d) of the Act

29 June 2015

Cancellation by sponsor

Requested by Biomet Australia Pty Ltd
Biomet Australia Pty Ltd - Prosthesis, internal, joint, hip, acetabular support component Cancelled under Section 41GL(d) of the Act

29 June 2015

Cancellation by sponsor

Requested by Biomet Australia Pty Ltd
Biomet Australia Pty Ltd - Orthopaedic fixation plate, non-biodegradable Cancelled under Section 41GL(d) of the Act

29 June 2015

Cancellation by sponsor

Requested by Biomet Australia Pty Ltd
Biomet Australia Pty Ltd - Orthopaedic fixation plate, non-biodegradable Cancelled under Section 41GL(d) of the Act

29 June 2015

Cancellation by sponsor

Requested by Biomet Australia Pty Ltd
Biomet Australia Pty Ltd - Orthopaedic bone screw, non-biodegradable Cancelled under Section 41GL(d) of the Act

29 June 2015

Cancellation by sponsor

Requested by Biomet Australia Pty Ltd
Biomet Australia Pty Ltd - Fixation device, internal, nail, intramedullary, tibia Cancelled under Section 41GL(d) of the Act

29 June 2015

Cancellation by sponsor

Requested by Biomet Australia Pty Ltd
Prosthesis, internal, joint, hip, acetabular component ()

11 February 2015

Cancellation or suspension

Regulatory action due to , effective 11/02/2015
Prosthesis, internal, joint, hip, femoral component ()

11 February 2015

Cancellation or suspension

Regulatory action due to , effective 11/02/2015
Biomet Australia Pty Ltd - Prosthesis, hip, internal, femoral head component ()

11 February 2015

Cancellation or suspension

Regulatory action due to , effective 11/02/2015
CAD/CAM unit, orthopaedic [41018] (Cancelled under s.41GN(1)(f))

23 September 2013

Cancellation or suspension

Regulatory action due to As the sponsor failed to provide evidence that an appropriate conformity assessment procedure has been applied to the device, the certification made under s.41FD(f) was incorrect., effective 23/09/2013

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