FDA.reportPublic FDA data

CROSS-FUSE™* II PEEK VBR/IBF SYSTEM

Primary DI
00846468008390
Brand
CROSS-FUSE™* II PEEK VBR/IBF SYSTEM
Company
Pioneer Surgical Technology, Inc.
Model
38-1860-9
Catalog number
38-1860-9
Device description
Crossfuse II Implant, 18x60x9
Published
2015-12-21
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
MQPSPINAL VERTEBRAL BODY REPLACEMENT DEVICE

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MQPSpinal Vertebral Body Replacement DeviceOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00846468008390PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00846468008390008464680083908464680083900846468008390

GMDN Terms#

Term, Definition table
TermDefinition
Vertebral body prosthesisAn implantable device designed to replace one or more vertebral body(s) that has collapsed or been surgically removed due to trauma, tumour or degenerative disease. Also known as a corpectomy or vertebrectomy spacer, it is in the form of a one-piece or modular hollow cylinder made of inorganic materials (e.g., metal, polymer). It is typically used with supplemental spinal fixation and/or bone graft, and some types are adjustable for in situ adjustment of prosthesis height to allow intraoperative distraction of adjacent vertebrae.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(906)226-9909labeling@resolvesurg.com
+1(906)226-9909regulatory@exalta.com

Regulatory Flags#

DUNS number
793384496
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00840298701902CODA™ Anterior Cervical Plate System58-2022010102022-01-0102023-01-19
00840298701971CODA™ Anterior Cervical Plate System58-2022010242022-01-0242023-01-19
00840298702039CODA™ Anterior Cervical Plate System58-2022020282022-02-0282023-01-19
00840298702268CODA™ Anterior Cervical Plate System58-2022040802022-04-0802023-01-19
00840298700134CODA™ Anterior Cervical Plate System58-202221018S2022-21-018S2023-01-19
00840298700028CODA™ Anterior Cervical Plate System58-202220014S2022-20-014S2023-01-19
00840298700110CODA™ Anterior Cervical Plate System58-202221014S2022-21-014S2023-01-19
00840298700677CODA™ Anterior Cervical Plate System58-2022302002022-30-2002023-01-24
00840298701957CODA™ Anterior Cervical Plate System58-2022010202022-01-0202023-01-19
00840298702022CODA™ Anterior Cervical Plate System58-2022020262022-02-0262023-01-19
00840298702251CODA™ Anterior Cervical Plate System58-2022040762022-04-0762023-01-19
00840298700608CODA™ Anterior Cervical Plate System58-2022222002022-22-2002023-01-24
00840298700776CODA™ Anterior Cervical Plate System58-2022100072022-10-0072023-01-25
00840298700905CODA™ Anterior Cervical Plate System58-2022207172022-20-7172023-01-19
00840298701933CODA™ Anterior Cervical Plate System58-2022010162022-01-0162023-01-19
00840298701988CODA™ Anterior Cervical Plate System58-2022010262022-01-0262023-01-19
00840298702091CODA™ Anterior Cervical Plate System58-2022020402022-02-0402023-01-19
00840298702114CODA™ Anterior Cervical Plate System58-2022020442022-02-0442023-01-19
00840298702138CODA™ Anterior Cervical Plate System58-2022030452022-03-0452023-01-19
00840298702176CODA™ Anterior Cervical Plate System58-2022030572022-03-0572023-01-19

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
04052536212989ADDplusUlrich GmbH & Co. KGMQP2026-03-03
04052536212996ADDplusUlrich GmbH & Co. KGMQP2026-03-03
04052536213009ADDplusUlrich GmbH & Co. KGMQP2026-03-03
04052536213016ADDplusUlrich GmbH & Co. KGMQP2026-03-03
04052536213023ADDplusUlrich GmbH & Co. KGMQP2026-03-03
04052536212804Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212811Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212828Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212835Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212842Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212859Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212866Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212873Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212880Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212897Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212903Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212910Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212927Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212934Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212941Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212958Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212965Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
04052536212972Small VBR (ADD)Ulrich GmbH & Co. KGMQP2026-03-02
00763000857936T2 STRATOSPHERE™ Expandable Corpectomy SystemMEDTRONIC SOFAMOR DANEK, INC.MQP2026-02-27
00810141048478Foundation Surgical VertiwedgeFOUNDATION SURGICAL GROUP INCMQP2026-02-26
00810141048485Foundation Surgical VertiwedgeFOUNDATION SURGICAL GROUP INCMQP2026-02-26
00810141048492Foundation Surgical VertiwedgeFOUNDATION SURGICAL GROUP INCMQP2026-02-26
00810141048508Foundation Surgical VertiwedgeFOUNDATION SURGICAL GROUP INCMQP2026-02-26
00810141048515Foundation Surgical VertiwedgeFOUNDATION SURGICAL GROUP INCMQP2026-02-26
00810141048577Foundation Surgical VertiwedgeFOUNDATION SURGICAL GROUP INCMQP2026-02-26