Perimeter® Interbody Fusion Device

Spacer X0305157 Vrtbl XL ADD ON 8DEG18MM

Registry build 21.09.26
14manufacturers in China registered for this device type
124catalogue numbers in this listing
18510(k) clearances naming this product 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 Perimeter® Interbody Fusion Device
Listed by Medtronic Sofamor Danek, 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
510(k) K090353
Record published 2015-08-07
Record revised 2025-07-14 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Sizes Width 14 to 38 mm; length 15 to 28 mm; height 8 to 20 mm; angle 4 to 15 °
Distribution end date 2024-12-05

Catalogue Numbers

Catalogue numbers for Perimeter® Interbody Fusion Device
Catalogue number Size Status
3298114 MEDIUM, 14mm, 8DEG In distribution
3494320 Width 36.0 mm In distribution
3493316 Width 30.0 mm In distribution
X0910120 Width 36.0 mm In distribution
X0910111 Length 24.0 mm In distribution
3491214 Length 15.0 mm In distribution
X0305157 Width 36.0 mm In distribution
X0910094 Height 12.0 mm In distribution
X0910108 Width 30.0 mm In distribution
3492316 Length 21.0 mm In distribution
3494316 Width 36.0 mm In distribution
X0910117 Length 24.0 mm In distribution
3297110 SMALL, 10mm, 4DEG In distribution
X0910106 Width 30.0 mm In distribution
3492318 Width 26.0 mm In distribution
X0910110 Width 30.0 mm In distribution
3299220 LARGE, 20mm, 12DEG In distribution
X0910114 Width 30.0 mm In distribution
3493312 Width 30.0 mm In distribution
X0910113 Height 8.0 mm In distribution
X0910093 Width 26.0 mm In distribution
3493310 Angle 8.0 ° In distribution
3299108 LARGE, 8mm, 8DEG In distribution
X0305193 In distribution
3492320 Length 21.0 mm In distribution
X0910123 Width 36.0 mm In distribution
X1110084 Width 38.0 mm In distribution
3493318 Width 30.0 mm In distribution
X1110078 Height 14.0 mm In distribution
X0910133 Length 28.0 mm In distribution
X0910115 Height 12.0 mm In distribution
3299216 LARGE, 16mm, 12DEG In distribution
X0305195 In distribution
X0910129 Height 12.0 mm In distribution
3491212 Angle 4.0 ° In distribution
X0910122 Height 12.0 mm In distribution
3494318 Angle 8.0 ° In distribution
X0910121 Length 28.0 mm In distribution
X0910131 Width 36.0 mm In distribution
X0305152 Height 8.0 mm In distribution
3491210 Height 10.0 mm In distribution
3493320 Angle 8.0 ° In distribution
3493412 Height 12.0 mm In distribution
3493420 Angle 12.0 ° In distribution
3493418 Width 30.0 mm In distribution
X0910116 Height 14.0 mm In distribution
3299110 LARGE, 10mm, 8DEG In distribution
3492308 Length 21.0 mm In distribution
X0910112 Length 24.0 mm In distribution
3493414 Width 14.0 mm In distribution
3492310 Angle 8.0 ° In distribution
X0910109 Width 30.0 mm In distribution
X0910132 Height 18.0 mm In distribution
3299116 LARGE 16mm, 8DEG In distribution
X0910119 Width 30.0 mm In distribution
X0910107 Width 30.0 mm In distribution
X1110085 Height 14.0 mm In distribution
3493416 Length 16.0 mm In distribution
X0305194 In distribution
3492312 Length 21.0 mm In distribution
3297114 SMALL, 14mm, 4DEG In distribution
X0305196 In distribution
X0910118 Length 24.0 mm In distribution
3493308 Height 8.0 mm In distribution
3494310 Length 28.0 mm In distribution
X0305156 Angle 8.0 ° In distribution
3491208 Angle 4.0 ° In distribution
3298110 MEDIUM, 10mm, 8DEG In distribution
X0910128 Length 28.0 mm In distribution
X0910126 Width 36.0 mm In distribution
3492314 Height 14.0 mm In distribution
3494312 Angle 8.0 ° In distribution
3493314 Width 30.0 mm In distribution
X0910124 Length 28.0 mm In distribution
X0910130 Length 28.0 mm In distribution
3299214 LARGE, 14mm, 12DEG In distribution
3494314 Width 36.0 mm In distribution
3299118 LARGE, 18mm, 8DEG In distribution
X0910125 Height 18.0 mm In distribution
X1110070 Width 38.0 mm Withdrawn
X0910100 Height 10.0 mm Withdrawn
X0910104 Length 21.0 mm Withdrawn
3493516 15DEG x H=16mm x W=30mm x L=24mm Withdrawn
X0910098 Width 26.0 mm Withdrawn
X1110083 Width 38.0 mm Withdrawn
X1111492 Width 30.0 mm Withdrawn
X1111495 Width 30.0 mm Withdrawn
X1110073 Width 38.0 mm Withdrawn
X1111477 Angle 4.0 ° Withdrawn
X1110080 Width 38.0 mm Withdrawn
X1110072 Width 38.0 mm Withdrawn
X1110079 Height 16.0 mm Withdrawn
3493514 Length 24.0 mm Withdrawn
X1110081 Length 28.0 mm Withdrawn
X1110087 Length 28.0 mm Withdrawn
X0910101 Width 26.0 mm Withdrawn
X1110075 Length 28.0 mm Withdrawn
X1111499 Angle 12.0 ° Withdrawn
X1111491 Length 24.0 mm Withdrawn
X1111496 Height 13.0 mm Withdrawn
X0910096 Width 26.0 mm Withdrawn
X0910095 Height 14.0 mm Withdrawn
X1110074 Width 38.0 mm Withdrawn
X1110069 Length 28.0 mm Withdrawn
X0910099 Width 26.0 mm Withdrawn
X0910127 Height 8.0 mm Withdrawn
X1110076 Length 28.0 mm Withdrawn
X0910103 Length 21.0 mm Withdrawn
3493512 Angle 15.0 ° Withdrawn
X0910102 Length 21.0 mm Withdrawn
X1111498 Width 30.0 mm Withdrawn
X0910105 Width 26.0 mm Withdrawn
X1111494 Height 19.0 mm Withdrawn
X0910097 Height 18.0 mm Withdrawn
X1110077 Length 28.0 mm Withdrawn
X0910092 Width 26.0 mm Withdrawn
X1111493 Length 24.0 mm Withdrawn
X1110068 Width 38.0 mm Withdrawn
3493518 15DEG x H=18mm x W=30mm x L=24mm Withdrawn
X1110088 Height 20.0 mm Withdrawn
X1111497 Angle 12.0 ° Withdrawn
3493520 15DEG x H=20mm x W=30mm x L=24mm Withdrawn
X1110086 Width 38.0 mm Withdrawn
X1110071 Length 28.0 mm Withdrawn

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
K201267 2020-08-26
K172199 2017-09-19
K171031 2017-07-06
K171468 2017-06-13
K132897 2013-12-11
K133216 2013-11-22
K132700 2013-09-26
K123027 2013-07-25
K122037 2013-03-22
K122591 2012-09-18
K111525 2011-08-24
K103731 2011-07-18
K100175 2010-06-02
K094025 2010-04-26
K090353 2009-09-29
K083026 2008-12-29
K082342 2008-09-12
K080083 2008-04-10

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