TrellOss™-A

GUDID 00840067204863

ALIF Trial Caddy

NEXXT SPINE, LLC

Sterilization/disinfection container Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable
Primary Device ID00840067204863
NIH Device Record Keya187cc4f-0c07-4a73-8bbc-7c54d173d0b3
Commercial Distribution StatusIn Commercial Distribution
Brand NameTrellOss™-A
Version Model Number330H0003
Company DUNS003489810
Company NameNEXXT SPINE, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100840067204863 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


[00840067204863]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-04-01
Device Publish Date2020-03-24

On-Brand Devices [TrellOss™-A]

00840067204467ALIF Distractor Inserter
00840067204849Implant Remover
00840067204832Slap Hammer Adapter
00840067204825Slap Hammer
00840067204863ALIF Trial Caddy
00840067205655Inline Handle Hudson Conn
00840067205303ALIF 36Wx27Dx20H 20°
00840067205297ALIF 36Wx27Dx18H 20°
00840067205280ALIF 36Wx27Dx16H 20°
00840067205273ALIF 36Wx27Dx14H 20°
00840067205266ALIF 36Wx27Dx12H 20°
00840067205259ALIF 32Wx24Dx20H 20°
00840067205242ALIF 32Wx24Dx18H 20°
00840067205235ALIF 32Wx24Dx16H 20°
00840067205228ALIF 32Wx24Dx14H 20°
00840067205211ALIF 32Wx24Dx12H 20°
00840067205204ALIF 36Wx27Dx20H 14°
00840067205198ALIF 36Wx27Dx18H 14°
00840067205181ALIF 36Wx27Dx16H 14°
00840067205174ALIF 36Wx27Dx14H 14°
00840067205167ALIF 36Wx27Dx12H 14°
00840067205150ALIF 36Wx27Dx10H 14°
00840067205143ALIF 32Wx24Dx20H 14°
00840067205136ALIF 32Wx24Dx18H 14°
00840067205129ALIF 32Wx24Dx16H 14°
00840067205112ALIF 32Wx24Dx14H 14°
00840067205105ALIF 32Wx24Dx12H 14°
00840067205099ALIF 32Wx24Dx10H 14°
00840067205082ALIF 36Wx27Dx20H 8°
00840067205075ALIF 36Wx27Dx18H 8°
00840067205068ALIF 36Wx27Dx16H 8°
00840067205051ALIF 36Wx27Dx14H 8°
00840067205044ALIF 36Wx27Dx12H 8°
00840067205037ALIF 36Wx27Dx10H 8°
00840067205020ALIF 36Wx27Dx8H 8°
00840067205013ALIF 32Wx24Dx20H 8°
00840067205006ALIF 32Wx24Dx18H 8°
00840067204993ALIF 32Wx24Dx16H 8°
00840067204986ALIF 32Wx24Dx14H 8°
00840067204979ALIF 32Wx24Dx12H 8°
00840067204962ALIF 32Wx24Dx10H 8°
00840067204955ALIF 32Wx24Dx8H 8°
00840067204870ALIF Implant Inserter
00840067204818Trial 27Dx36Wx20H 20°
00840067204801Trial 27Dx36Wx18H 20°
00840067204795Trial 27Dx36Wx16H 20°
00840067204788Trial 27Dx36Wx14H 20°
00840067204771Trial 27Dx36Wx12H 20°
00840067204764Trial 27Dx36Wx20H 14°
00840067204757Trial 27Dx36Wx18H 14°

Trademark Results [TrellOss]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TRELLOSS
TRELLOSS
88401530 not registered Live/Pending
Zimmer Biomet Spine, Inc.
2019-04-25

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