Sypher Alif Spacer System

Sypher Locking Cover Plate - 32mm X 12mm. Prohibits Bone Screw backout after implantation.

Registry build 21.09.26
14manufacturers in China registered for this device type
43catalogue numbers in this listing
1510(k) clearance

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 Sypher Alif Spacer System
Listed by Biogennix, LLC, 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 Specification developer, Repacker / relabeller, Manufacturer
510(k) K141798
Record published 2016-12-19
Record revised 2024-09-11 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, serial number
Sizes Height 12 to 18 mm; width 28 to 38 mm; angle 7 to 12 °; depth 24 to 29 mm; length 25 to 35 mm; outer diameter 5 to 6 mm; width 28 Nanometer

Catalogue Numbers

Catalogue numbers for Sypher Alif Spacer System
Catalogue number Size Status
SAS-38291807 Angle 7 ° In distribution
SAS-38291207 Angle 7 ° In distribution
SAS-32261407 Angle 7 ° In distribution
SAS-5035 Length 35 mm In distribution
SAS-32261607 Angle 7 ° In distribution
SAS-35261412 Angle 12 ° In distribution
SAS-28241407 Angle 7 ° In distribution
SAS-35261807 Angle 7 ° In distribution
SAS-28241612 Angle 12 ° In distribution
SAS-32261207 Angle 7 ° In distribution
SAS-28241207 Angle 7 ° In distribution
SAS-35261612 Angle 12 ° In distribution
SAS-28241212 Angle 12 ° In distribution
SAS-35261212 Angle 12 ° In distribution
SAS-5535 Length 35 mm In distribution
SAS-38291612 Angle 12 ° In distribution
SAS-32261812 Angle 12 ° In distribution
SAS-38291407 Angle 7 ° In distribution
SAS-5530 Length 30 mm In distribution
SAS-28241807 Angle 7 ° In distribution
SAS-6035 Length 35 mm In distribution
SAS-35261812 Angle 12 ° In distribution
SAS-5030 Length 30 mm In distribution
SAS-5525 Length 25 mm In distribution
SAS-5025 Length 25 mm In distribution
SAS-35261207 Angle 7 ° In distribution
SAS-32261212 Angle 12 ° In distribution
SAS-28241812 Angle 12 ° In distribution
SAS-28241607 Angle 7 ° In distribution
SAS-38291212 Angle 12 ° In distribution
SAS-35261607 Angle 7 ° In distribution
SAS-32261412 Angle 12 ° In distribution
SAS-28241412 Angle 12 ° In distribution
SAS-38291607 Angle 7 ° In distribution
SAS-32261807 Angle 7 ° In distribution
SAS-38291412 Angle 12 ° In distribution
SAS-32261612 Angle 12 ° In distribution
SAS-6025 Length 25 mm In distribution
SAS-6030 Length 30 mm In distribution
SAS-3212 Height 12 mm In distribution
SAS-2812 Height 12 mm In distribution
SAS-38291812 Angle 12 ° In distribution
SAS-35261407 Angle 7 ° 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
K181337 2018-09-18

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