WENZEL SPINE, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30080098503008009850WENZEL SPINE, Inc.1N2020-04-251130 Rutherford Lane Suite 200 Austin TX US 78753

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00813210020009VariLift-L - The Wenzel Spine VariLift Lumbar Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-L is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-L is designed to be implanted bi-laterally via posterior (PLIF) approach or as a single device via a transverse (TLIF) approach. VariLift-L may be implanted with or without supplemental fixation and is intended for use with autograft to facilitate fusion. VariLift-L is indicated for intervertebral body fusion of the lumbar spine, from L2 to S1, in skeletally mature patients who have had six months of non-operative treatment. The device is intended for use at either one level or two contiguous levels for the treatment of degenerative disc disease (DDD) with up to Grade 1 spondylolisthesis. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies.855-936-9351info@wenzelspine.com
00813210020016VariLift-L - The Wenzel Spine VariLift Lumbar Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-L is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-L is designed to be implanted bi-laterally via posterior (PLIF) approach or as a single device via a transverse (TLIF) approach. VariLift-L may be implanted with or without supplemental fixation and is intended for use with autograft to facilitate fusion. VariLift-L is indicated for intervertebral body fusion of the lumbar spine, from L2 to S1, in skeletally mature patients who have had six months of non-operative treatment. The device is intended for use at either one level or two contiguous levels for the treatment of degenerative disc disease (DDD) with up to Grade 1 spondylolisthesis. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies.855-936-9351info@wenzelspine.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1100241146917381K151900VariLift-L Interbody Fusion DeviceMAX2015-12-11
1100241520775765K131296VARILIFT-L INTERBODY FUSION DEVICEMAX2013-09-03
1100241452407044K120603VARILIFT -CODP2013-01-29
1100241361512159K111123VARILIFT CERVICAL INTERBODY FUSION SYSTEMODP2011-12-08
1100241983676833K102438PRIMALOK FACET FIXATION SYSTEMMRW2010-09-30
1100241305169931K100820WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEMMAX2010-08-05
1100241613069402K100354PRIMAL OK INTERSPINOUS FUSION SYSTEMKWP2010-08-17
1100242045541059K030608OTI BONE CEMENT PLUGJDK2003-06-12

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MAX32015-12-11
ODP22013-01-29
MRW12010-09-30
KWP12010-08-17
JDK12003-06-12

PMN#

GUDID#

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