SeaSpine Spacer System – Hollywood™

Hollywood VI Implant, 11mm x 27mm x 12mm, Lordotic

Registry build 21.09.26
3manufacturers in China registered for this device type
74catalogue numbers in this listing

Who Else Makes It

Concentrated in Shanghai (1), Jiangsu (1), Shandong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code MQP
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53

Record

Regulatory record for SeaSpine Spacer System – Hollywood™
Listed by Seaspine Orthopedics Corporation, United States
FDA product code MQP
Device type Spinal Vertebral Body Replacement Device
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K052170
Record published 2016-11-09
Record revised 2025-10-24 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Distribution end date 2016-09-02
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for SeaSpine Spacer System – Hollywood™
Catalogue number Size Status
93-4215 11mm x 30mm x 15mm In distribution
93-4182 12mm In distribution
93-4209 11mm x 30mm x 9mm In distribution
34-8012 11mm x 27mm x 12mm In distribution
34-9012 11mm x 30mm x 12mm In distribution
93-4185 15mm In distribution
93-4236 12mm In distribution
93-4187 17mm In distribution
93-4178 8mm In distribution
34-8013 11mm x 27mm x 13mm In distribution
34-9011 11mm x 30mm x 11mm In distribution
93-4213 11mm x 30mm x 13mm In distribution
34-5017 11mm x 27mm x 17mm In distribution
93-4257 14mm In distribution
93-4186 16mm In distribution
93-4234 10mm In distribution
34-9016 11mm x 30mm x 16mm In distribution
93-4259 16mm In distribution
93-4241 17mm In distribution
34-8009 11mm x 27mm x 9mm In distribution
93-4260 17mm In distribution
93-4253 10mm In distribution
93-4188 18mm In distribution
93-4201 N/A In distribution
34-8007 11mm x 27mm x 7mm In distribution
93-4256 13mm In distribution
93-4238 14mm In distribution
93-4177 7mm In distribution
93-4231 7mm In distribution
93-4180 10mm In distribution
34-9010 11mm x 30mm x 10mm In distribution
93-4183 13mm In distribution
34-9018 11mm x 30mm x 18mm In distribution
34-5009 11mm x 27mm x 9mm In distribution
93-4233 9mm In distribution
34-5018 11mm x 27mm x 18mm In distribution
34-9017 11mm x 30mm x 17mm In distribution
34-5012 11mm x 27mm x 12mm In distribution
34-8015 11mm x 27mm x 15mm In distribution
34-5013 11mm x 27mm x 13mm In distribution
34-9015 11mm x 30mm x 15mm In distribution
93-4258 15mm In distribution
93-4251 8mm In distribution
93-4211 11mm x 30mm x 11mm In distribution
34-5015 11mm x 27mm x 15mm In distribution
93-4181 11mm In distribution
34-9013 11mm x 30mm x 13mm In distribution
93-4184 14mm In distribution
93-4179 9mm In distribution
34-8016 11mm x 27mm x 16mm In distribution
34-5012 11mm x 27mm x 12mm Withdrawn
34-5007 11mm x 27mm x 7mm Withdrawn
34-5018 11mm x 27mm x 18mm Withdrawn
34-5015 11mm x 27mm x 15mm Withdrawn
34-5011 11mm x 27mm x 11mm Withdrawn
93-4178 8mm Withdrawn
93-4182 12mm Withdrawn
93-4177 7mm Withdrawn
34-5010 11mm x 27mm x 10mm Withdrawn
34-5008 11mm x 27mm x 8mm Withdrawn
93-4185 15mm Withdrawn
93-4184 14mm Withdrawn
34-5009 11mm x 27mm x 9mm Withdrawn
34-5014 11mm x 27mm x 14mm Withdrawn
34-5017 11mm x 27mm x 17mm Withdrawn
93-4187 17mm Withdrawn
93-4181 11mm Withdrawn
34-5016 11mm x 27mm x 16mm Withdrawn
34-5013 11mm x 27mm x 13mm Withdrawn
93-4188 18mm Withdrawn
93-4180 10mm Withdrawn
93-4183 13mm Withdrawn
93-4179 9mm Withdrawn
93-4186 16mm Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
CoRoent Nuvasive, Inc. 1,514
Capri™ Corpectomy Cage System VB Spine LLC 1,509
Aleutian® Interbody Systems VB Spine LLC 1,189
Fortify Globus Medical, Inc. 866
Matrixx System Nexxt Spine LLC 748
Ascend Alphatec Spine, Inc. 555
Zavation VBR Trial Zavation 548
Verte-Stack® Spinal System Medtronic Sofamor Danek, Inc. 484
Timberline® Lateral Interbody Fusion System Biomet Spine 470
Timberline Lateral Fusion System Biomet Spine 459
Novel Alphatec Spine, Inc. 447
Hawkeye™ Vertebral Body Replacement (VBR) Choice Spine, LP 368

Showing 12 of 683. All products under Spinal Vertebral Body Replacement Device

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