11 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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neoClose AnchorGuide Regular Port Closure Kit US
FDA UDI
NEOSURGICAL LIMITED·05391529640026·Laparoscopy wound closure system kit consists o...
neoClose AnchorGuard
FDA UDI
NEOSURGICAL LIMITED·05391529640460·Laparoscopy wound closure system guide consists...
neoClose AnchorGuide 5/15 Port Closure Kit US (2 Port)
FDA UDI
NEOSURGICAL LIMITED·05391529640224·Laparoscopy wound closure system kit consists o...
neoClose AnchorGuide 8/15 Port Closure Kit US (1 Port)
FDA UDI
NEOSURGICAL LIMITED·05391529640194·Laparoscopy wound closure system kit consists o...
neoClose AnchorGuide 5/12 Port Closure Kit US (1 Port)
FDA UDI
NEOSURGICAL LIMITED·05391529640163·Laparoscopy wound closure system kit consists o...
neoClose 2 AutoAnchor Pack US
FDA UDI
NEOSURGICAL LIMITED·05391529640101·Laparoscopy wound closure system pack consists ...
neoClose 2 Anchor (Long Driver) US
FDA UDI
NEOSURGICAL LIMITED·05391529640552·Laparoscopy wound closure system pack consists ...
neoClose 4 AutoAnchor Pack US
FDA UDI
NEOSURGICAL LIMITED·05391529640125·Laparoscopy wound closure system pack consists ...
neoClose AnchorGuide XL Port Closure Kit US
FDA UDI
NEOSURGICAL LIMITED·05391529640064·Laparoscopy wound closure system kit consists o...
neoClose AnchorGuide Regular Port Closure Kit x2 US
FDA UDI
NEOSURGICAL LIMITED·05391529640088·Laparoscopy wound closure system kit consists o...
Sequoia final driver closure top retention, non-sterile, REF 3384-2, Zimmer Spine, Austin, Texas, The device is used to apply final torque to closure tops of the implant. The Sequoia Final Driver is used in conjunction with a counter torque tube to apply final torque to closure tops that secure the rod component to the screw head component until the torque limiting handle pops once, indicating the implant has been locked. This process is repeated with all closure tops in a construct (assembly). The Sequoia Final Driver is also used to tighten the set screw feature and lateral locking cams on the SpeedLinkII transverse connectors when used and is used to remove previously inserted closure tops during construct removal.
FDA Recall
Terminated
·Zimmer Inc.·Product code HAO·April 4, 2011