FDA.reportPublic FDA data

tezo-P™ titanium cage family

Primary DI
04052536077175
Brand
tezo-P™ titanium cage family
Company
Ulrich GmbH & Co. KG
Model
CS 3403-11
Catalog number
CS 3403-11
Device description
tezo-P, height 11 mm, length 29 mm, angle 12°
Published
2016-07-30
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
MAXIntervertebral fusion device with bone graft, lumbar

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K122957000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K122957000TEZO TITANIUM CAGE FAMILYUlrich GmbH & Co. KG2013-06-21MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04052536077175PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04052536077175040525360771754052536077175

GMDN Terms#

Term, Definition table
TermDefinition
Metallic spinal interbody fusion cageA device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+4907319654152safety@ulrichmedical.com
+4973196540safety@ulrichmedical.com

Regulatory Flags#

DUNS number
315494757
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04052536085330neon3CS 3922-4102026-05-28
04052536085361neon3CS 3924-4102026-05-28
04052536085491neon3CS 39302026-05-28
04052536085507neon3CS 39312026-05-28
04052536085552neon3CS 39342026-05-28
04052536161836neon3CS 3926-032026-05-28
04052536161867neon3CS 3927-032026-05-28
04052536161959neon3CS 3936-012026-05-28
04052536161966neon3CS 3937-032026-05-28
04052536161973neon3CS 3937-042026-05-28
04052536161775neon3CS 3920-012026-05-26
04052536216710neon3CS 3921-012026-05-26
04052536085323N/ACS 3921-02CS 3921-022016-09-22
04052536085347N/ACS 3923-01CS 3923-012016-09-22
04052536085354N/ACS 3923-02CS 3923-022016-09-22
04052536085460N/ACS 3929-02CS 3929-022016-09-22
04052536085484N/ACS 3929-04CS 3929-042016-09-22
04052536085521N/ACS 3932-02CS 3932-022016-09-22
04052536085545N/ACS 3933CS 39332016-09-22
04052536161782neon³ CT spinal stabilizationCS 3925-01CS 3925-012016-09-22

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00197157076023ZAVATION DISTRACTORZavation LLCMAX2026-05-28
00197157076030ZAVATION DISTRACTORZavation LLCMAX2026-05-28
00197157076047ZAVATION DISTRACTORZavation LLCMAX2026-05-28
00197157076054ZAVATION DISTRACTORZavation LLCMAX2026-05-28
00197157076061ZAVATION DISTRACTORZavation LLCMAX2026-05-28
00197157075859ZAVATION INSERTERZavation LLCMAX2026-05-27
00810166522366X-PACEXPANDING INNOVATIONS, INC.MAX2026-05-27
00810166522373X-PACEXPANDING INNOVATIONS, INC.MAX2026-05-27
B70712535005S0Dual X Graft Tamp ShortAMPLIFY SURGICAL, INC.MAX2026-05-27
B707129410010130DUALXS T/PLIF 15 DEG x 9-12MMAMPLIFY SURGICAL, INC.MAX2026-05-27
B707129410010200DUALXS T/PLIF 18 DEG x 10-13MMAMPLIFY SURGICAL, INC.MAX2026-05-27
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