Signature

SIGNATURE TLIF TPS Spacer, MIS, Small, 10mm

Registry build 21.09.26
14manufacturers in China registered for this device type
135catalogue numbers in this listing
20510(k) clearances naming this product code
22recalls on this code

Who Else Makes It

Concentrated in Jiangsu (6), Shandong (2), Shanghai (2). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MAX
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Jiangsu Ideal Medical Science & Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shanghai Reach Medical Instrument Co., Ltd. Shanghai Shanghai Manufacturer 30
Changzhou Geasure Medical Apparatus AND Instruments Co., Ltd. Changzhou Jiangsu Contract manufacturer 25
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Showing 12 of 14. All 14 manufacturers in China registered for Intervertebral Fusion Device With Bone Graft, Lumbar

Record

Regulatory record for Signature
Listed by Globus Medical, Inc., United States
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Manufacturer, Exporter
510(k) K143578
Record published 2020-03-08
Record revised 2025-07-14 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date
Sizes Length 28 to 33 mm; width 10 to 11 mm; height 7 to 17 mm

Catalogue Numbers

Catalogue numbers for Signature
Catalogue number Size Status
368.210CS Length 28 mm In distribution
368.254 Width 10 mm In distribution
168.255 Length 28 mm In distribution
368.215 Height 15 mm In distribution
368.328 Height 8 mm In distribution
168.253 Height 13 mm In distribution
368.309CS Length 33 mm In distribution
168.355 Length 33 mm In distribution
368.230CS Height 10 mm In distribution
168.357 Height 17 mm In distribution
368.350 Height 10 mm In distribution
368.307CS Height 7 mm In distribution
368.235CS Height 15 mm In distribution
368.409 Length 28 mm In distribution
368.352 Length 33 mm In distribution
368.312 Length 33 mm In distribution
368.236 Width 10 mm In distribution
368.234 Width 10 mm In distribution
168.247 Length 28 mm In distribution
368.229 Length 28 mm In distribution
368.336 Length 33 mm In distribution
368.228 Width 10 mm In distribution
168.256 Height 16 mm In distribution
368.317CS Length 33 mm In distribution
368.313 Width 11 mm In distribution
168.252 Width 10 mm In distribution
368.213CS Length 28 mm In distribution
368.335CS Height 15 mm In distribution
168.352 Length 33 mm In distribution
368.417 Height 17 mm In distribution
368.335 Length 33 mm In distribution
368.215CS Height 15 mm In distribution
168.347 Height 7 mm In distribution
368.333CS Height 13 mm In distribution
368.233CS Height 13 mm In distribution
368.408 Width 10 mm In distribution
368.316 Height 16 mm In distribution
368.233 Width 10 mm In distribution
368.353 Length 33 mm In distribution
368.332 Length 33 mm In distribution
368.309 Length 33 mm In distribution
368.410 Length 28 mm In distribution
368.214 Width 10 mm In distribution
368.411 Length 28 mm In distribution
368.308 Width 11 mm In distribution
368.330CS Length 33 mm In distribution
368.231CS Length 28 mm In distribution
368.249 Width 10 mm In distribution
368.355 Width 11 mm In distribution
368.210 Width 10 mm In distribution
368.333 Width 11 mm In distribution
368.314 Width 11 mm In distribution
168.249 Width 10 mm In distribution
368.257 Length 28 mm In distribution
168.248 Length 28 mm In distribution
368.329CS Width 11 mm In distribution
368.214CS Height 14 mm In distribution
368.332CS Length 33 mm In distribution
368.231 Length 28 mm In distribution
368.208CS Height 8 mm In distribution
368.310CS Length 33 mm In distribution
368.237 Width 10 mm In distribution
368.208 Width 10 mm In distribution
368.251 Length 28 mm In distribution
368.209 Length 28 mm In distribution
368.250 Height 10 mm In distribution
168.251 Length 28 mm In distribution
368.314CS Length 33 mm In distribution
368.307 Height 7 mm In distribution
368.331CS Width 11 mm In distribution
368.327 Width 11 mm In distribution
368.327CS Height 7 mm In distribution
368.256 Width 10 mm In distribution
368.235 Width 10 mm In distribution
368.216 Height 16 mm In distribution
368.248 Width 10 mm In distribution
368.211 Height 11 mm In distribution
368.315CS Width 11 mm In distribution
368.229CS Height 9 mm In distribution
368.356 Height 16 mm In distribution
368.334 Length 33 mm In distribution
368.348 Width 11 mm In distribution
368.207 Width 10 mm In distribution
368.413 Width 10 mm In distribution
368.227 Length 28 mm In distribution
368.209CS Height 9 mm In distribution
368.308CS Width 11 mm In distribution
168.348 Width 11 mm In distribution
368.313CS Width 11 mm In distribution
368.312CS Height 12 mm In distribution
368.311CS Width 11 mm In distribution
368.213 Width 10 mm In distribution
368.407 Width 10 mm In distribution
168.354 Width 11 mm In distribution
368.311 Length 33 mm In distribution
168.353 Height 13 mm In distribution
168.250 Length 28 mm In distribution
368.232CS Width 10 mm In distribution
168.254 Height 14 mm In distribution
368.217CS Length 28 mm In distribution
368.227CS Width 10 mm In distribution
368.329 Length 33 mm In distribution
368.317 Height 17 mm In distribution
368.230 Height 10 mm In distribution
168.356 Length 33 mm In distribution
368.310 Width 11 mm In distribution
368.331 Width 11 mm In distribution
368.412 Height 12 mm In distribution
368.211CS Length 28 mm In distribution
368.217 Length 28 mm In distribution
368.357 Length 33 mm In distribution
368.252 Height 12 mm In distribution
368.337CS Width 11 mm In distribution
168.351 Height 11 mm In distribution
368.415 Width 10 mm In distribution
368.207CS Length 28 mm In distribution
368.351 Length 33 mm In distribution
368.354 Height 14 mm In distribution
368.330 Length 33 mm In distribution
368.228CS Height 8 mm In distribution
368.347 Height 7 mm In distribution
368.315 Length 33 mm In distribution
168.349 Height 9 mm In distribution
368.253 Length 28 mm In distribution
368.328CS Length 33 mm In distribution
368.237CS Width 10 mm In distribution
368.247 Width 10 mm In distribution
368.255 Width 10 mm In distribution
168.350 Width 11 mm In distribution
368.212 Height 12 mm In distribution
368.212CS Width 10 mm In distribution
168.257 Length 28 mm In distribution
368.337 Length 33 mm In distribution
368.349 Width 11 mm In distribution
368.232 Width 10 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Peridot Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 10,850
Yellowstone Summit Spine 6,654
CoRoent Nuvasive, Inc. 5,690
Zavation Zavation 2,554
Anyplus II Spinal Fixation System GS Medical Co., Ltd. 2,533
Talos® IBF Meditech Spine, LLC 2,163
Peridot-PT Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 1,956
TirboLOX-L Lumbar Ibfd Captiva Spine, Inc. 1,926
Endoskeleton® TL Titan Spine, LLC 1,896
Evos Lumbar Interbody System Cutting Edge Spine 1,871
Epiphany Pantheon Spinal LLC 1,507
LnK Lumbar Interbody Fusion Cage System L&K Biomed Co., Ltd. 1,506

Showing 12 of 1,958. All products under Intervertebral Fusion Device With Bone Graft, Lumbar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K234035 2024-09-06
K221894 2023-08-03
K203278 2021-02-02
K192115 2020-01-14
K191391 2019-09-18
K181357 2018-12-06
K171848 2017-12-21
K152022 2017-02-22
K143578 2016-04-13
K151665 2016-03-16
K140411 2014-07-01
K130478 2013-07-26
K123913 2013-05-13
K123231 2013-01-18
K122097 2012-12-06
K113447 2012-01-26
K102293 2011-01-05
K102313 2010-12-03
K093242 2009-12-23
K072970 2008-01-18

Recalls

22 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Closed
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19
2020-07-22 Class II Nonconforming Material/Component Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy. 2021-08-19

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P000028 2004-06-18 AFFINITY ANTERIOR CERVICAL CAGE SYSTEM Medtronic Sofamor Danek USA, Inc.
P970015 2003-09-10 LT-CAGE PEEK LUMBAR TAPERED FUSION DEVICE Sofamor Danek
P980048 2001-04-20 BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM Sulzer Spine-Tech
P950019 1999-03-19 RAY THREADED FUSION CAGE (TFC) DEVICE WITH INSTRUMENTATION Stryker Spine
P950002 1997-06-30 BAK INTERBODY FUSION SYSTEM Zimmer Spine, Inc.

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer