BP® 8002-1524-00

GUDID 00889024338555

ZIMMER SPINE, INC.

Intervertebral-body internal spinal fixation system Intervertebral-body internal spinal fixation system Intervertebral-body internal spinal fixation system Intervertebral-body internal spinal fixation system Intervertebral-body internal spinal fixation system Intervertebral-body internal spinal fixation system Intervertebral-body internal spinal fixation system Intervertebral-body internal spinal fixation system Intervertebral-body internal spinal fixation system Intervertebral-body internal spinal fixation system Intervertebral-body internal spinal fixation system Intervertebral-body internal spinal fixation system Intervertebral-body internal spinal fixation system Intervertebral-body internal spinal fixation system
Primary Device ID00889024338555
NIH Device Record Key73dff978-b4d7-4641-b3f5-038bfd6f4ac6
Commercial Distribution StatusIn Commercial Distribution
Brand NameBP®
Version Model Number8002-1524-00
Catalog Number8002-1524-00
Company DUNS787663400
Company NameZIMMER SPINE, INC.
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com

Device Dimensions

Length24 Millimeter
Outer Diameter15 Millimeter
Length24 Millimeter
Outer Diameter15 Millimeter
Length24 Millimeter
Outer Diameter15 Millimeter
Length24 Millimeter
Outer Diameter15 Millimeter
Length24 Millimeter
Outer Diameter15 Millimeter
Length24 Millimeter
Outer Diameter15 Millimeter
Length24 Millimeter
Outer Diameter15 Millimeter
Length24 Millimeter
Outer Diameter15 Millimeter
Length24 Millimeter
Outer Diameter15 Millimeter
Length24 Millimeter
Outer Diameter15 Millimeter
Length24 Millimeter
Outer Diameter15 Millimeter
Length24 Millimeter
Outer Diameter15 Millimeter
Length24 Millimeter
Outer Diameter15 Millimeter
Length24 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024338555 [Primary]

FDA Product Code

MAXIntervertebral fusion device with bone graft, lumbar

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-12-03
Device Publish Date2015-09-24

On-Brand Devices [BP®]

0088902432074107.00008.047
0088902432073407.00008.046
0088902432072707.00008.039
0088902432071007.00008.038
0088902432070307.00008.031
0088902432069707.00008.030
0088902432068007.00008.023
0088902432067307.00008.022
0088902432066607.00008.015
0088902432065907.00008.014
0088902432064207.00008.007
008890243385798002-1724-00
008890243385628002-1720-00
008890243385558002-1524-00
008890243385488002-1520-00

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