Aero-C

Specialty Aero-C Pilot Cutter and Anchor Tamp

Registry build 21.09.26
7manufacturers in China registered for this device type
48catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Shanghai (2), Shandong (2), Zhejiang (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code ODP
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10
Shanghai Sanyou Medical Co., Ltd. Shanghai Shanghai Manufacturer 6

Record

Regulatory record for Aero-C
Listed by Stryker GmbH, Switzerland
FDA product code ODP
Device type Intervertebral Fusion Device With Bone Graft, Cervical
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2016-01-28
Record revised 2024-09-11 (version 8)

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, expiry date, manufacturing date
Sizes Height 5 to 10 mm; depth 12 to 16 mm; width 14 to 17 mm; angle 0 to 6 °
Distribution end date 2024-11-08
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Aero-C
Catalogue number Size Status
48894050 Width 15.0 mm In distribution
48892096 Angle 6.0 ° In distribution
48896096 Depth 16.0 mm In distribution
48980009 Height 9.0 mm In distribution
48896050 Angle 0.0 ° In distribution
48894086 Angle 6.0 ° In distribution
48896066 Depth 16.0 mm In distribution
48892086 Height 8.0 mm In distribution
48980008 Height 8.0 mm In distribution
48894066 Width 15.0 mm In distribution
48892076 Angle 6.0 ° In distribution
48980007 Height 7.0 mm In distribution
IS4540AER In distribution
48894076 Width 15.0 mm In distribution
48980006 Height 6.0 mm In distribution
48980002 In distribution
48892050 Width 14.0 mm In distribution
48896086 Height 8.0 mm In distribution
48892066 Depth 12.0 mm In distribution
48894096 Depth 14.0 mm In distribution
48896076 Depth 16.0 mm In distribution
48896090 Width 17.0 mm Withdrawn
48896080 Height 8.0 mm Withdrawn
48892000 Depth 12.0 mm Withdrawn
48890010 Withdrawn
48890009 Withdrawn
48894070 Depth 14.0 mm Withdrawn
48892106 Width 14.0 mm Withdrawn
48894106 Height 10.0 mm Withdrawn
48896100 Width 17.0 mm Withdrawn
48890007 Withdrawn
48896070 Width 17.0 mm Withdrawn
48894000 Depth 14.0 mm Withdrawn
48896000 Depth 16.0 mm Withdrawn
48892090 Height 9.0 mm Withdrawn
48892060 Width 14.0 mm Withdrawn
48892080 Width 14.0 mm Withdrawn
48896060 Height 6.0 mm Withdrawn
48894100 Depth 14.0 mm Withdrawn
48890008 Withdrawn
48892070 Width 14.0 mm Withdrawn
48894080 Height 8.0 mm Withdrawn
48890006 Withdrawn
48896106 Angle 6.0 ° Withdrawn
48892100 Width 14.0 mm Withdrawn
48894060 Angle 0.0 ° Withdrawn
48890002 Withdrawn
48894090 Depth 14.0 mm Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Latitude-C AM™ Cervical Interbody Fusion System Degen Medical 1,529
IdentiTi Alphatec Spine, Inc. 1,390
Zavation Zavation 1,357
IVA Cage Ti Diomedical Co., Ltd. 1,202
Latitude-C Cervical Interbody Spacer System Degen Medical 1,185
Peridot Anterior Cervical Intervertebral Body Fusion System Gbs Commonwealth Co., Ltd. 1,056
Aleutian® Interbody Systems VB Spine LLC 1,017
Valeo Spacer System Sintx Technologies Inc. 918
Cascadia™ Interbody System VB Spine LLC 823
CoRoent Nuvasive, Inc. 815
Tyber Medical Tyber Medical 740
Matisse Anterior Cervical Interbody Fusion Cage System CTL Medical Corporation 577

Showing 12 of 938. All products under Intervertebral Fusion Device With Bone Graft, Cervical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K142251 2014-11-19

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