Sable

SABLE Spacer, 12x30, 10-18mm, 22°

Registry build 21.09.26
14manufacturers in China registered for this device type
39catalogue 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 Sable
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) K192115
Record published 2024-12-01
Record revised 2025-07-14 (version 2)

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 22 to 30 mm; width 10 mm; height 6 to 11 mm; angle 8 to 22 °

Catalogue Numbers

Catalogue numbers for Sable
Catalogue number Size Status
1172.4234S In distribution
1172.0013S In distribution
6172.0030 Length 30 mm In distribution
1172.4210S In distribution
1172.2221S Width 10 mm In distribution
6172.0001 In distribution
6172.0022 Length 22 mm In distribution
1172.4113S In distribution
1172.4121S In distribution
1172.2021S Angle 15 ° In distribution
1172.2121S Angle 15 ° In distribution
1172.2133S Width 10 mm In distribution
1172.4221S In distribution
1172.4110S In distribution
1172.2035S Angle 22 ° In distribution
1172.2213S Width 10 mm In distribution
1172.0021S In distribution
6172.0002 In distribution
1172.2224S Height 10 mm In distribution
6172.0026 Length 26 mm In distribution
1172.2110S Height 6 mm In distribution
1172.4133S In distribution
1172.2124S Angle 15 ° In distribution
1172.4124S In distribution
1172.4213S In distribution
1172.0010S In distribution
1172.2013S Angle 8 ° In distribution
1172.2234S Height 10 mm In distribution
1172.2010S Height 6 mm In distribution
1172.4224S In distribution
1172.2113S Angle 8 ° In distribution
1172.2033S Length 22 mm In distribution
1172.0033S In distribution
6172.0005 In distribution
1172.2210S Angle 8 ° In distribution
1172.0035S In distribution
1172.0024S In distribution
1172.2024S Height 10 mm In distribution
6172.0101 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