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25 devices found
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Manufacturer: Vertiflex, Inc.
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Device · Manufacturer · Authorizations
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Status
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Registry
Class
Superion Retractor 100-9126
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Interspinous Spacer 14mm
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Sterilization Tray 100-9119
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Interspinous Spacer 8mm
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Grasping Forceps 100-9112
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Handle 100-9139
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Dilator 1, Blunt 100-9135
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Interspinous Spacer 12mm
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Interspinous Spacer 16mm
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Interspinous Spacer 10mm
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Dilator 2 100-9136
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Cannula 100-9137
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Dilator 1 100-9146
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Driver 100-9108
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Mallet 100-9127
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Inserter 100-9110
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Interspinous Reamer 100-9117
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Superion Interspinous Gauge 100-9115
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
GUDID
not on market
Withdrawn
GUDID
III
Modified Vertiflex Spinal Screw System
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K073143
Active
Cleared 7 Apr 2008
Active
510(k)
510(k)
II
Vertiflex Spinous Process Fixation Plate
Vertiflex, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K122509
Active
Cleared 17 Dec 2012
Active
510(k)
510(k)
II
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