CxHA™ CH141709

GUDID M711CH1417091

HA PEEK, Ta

INNO Holdings, Inc.

Polymeric spinal fusion cage, sterile

• Primary Device ID: M711CH1417091
• NIH Device Record Key: 0682b539-d480-4365-879e-c2ae390ce6cc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CxHA™
• Version Model Number: CH141709
• Catalog Number: CH141709
• Company DUNS: 141620464
• Company Name: INNO Holdings, Inc.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com

Device Dimensions

• Angle: 8 degree
• Height: 9 Millimeter
• Width: 17 Millimeter
• Length: 14 Millimeter
• Angle: 8 degree
• Height: 9 Millimeter
• Width: 17 Millimeter
• Length: 14 Millimeter
• Angle: 8 degree
• Height: 9 Millimeter
• Width: 17 Millimeter
• Length: 14 Millimeter
• Angle: 8 degree
• Height: 9 Millimeter
• Width: 17 Millimeter
• Length: 14 Millimeter
• Angle: 8 degree
• Height: 9 Millimeter
• Width: 17 Millimeter
• Length: 14 Millimeter
• Angle: 8 degree
• Height: 9 Millimeter
• Width: 17 Millimeter
• Length: 14 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M711CH1417090 [Primary]
HIBCC	M711CH1417091 [Package]; Contains: M711CH1417090; Package: Carton [1 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181115

FDA Product Code

• ODP: Intervertebral Fusion Device With Bone Graft, Cervical

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-12-17
• Device Publish Date: 2018-09-30

On-Brand Devices [CxHA™]

• M711LS4590: Polypropylene
• M711LS457080: SST
• M711LS457070: SST
• M711LS457060: SST
• M711LS457050: SST
• M711LS457040: SST
• M711LS457030: SST
• M711LS457020: SST
• M711LS457010: SST
• M711LS4550: SST
• M711LS4540: SST
• M711CH1417091: HA PEEK, Ta