FDA UDI Not in Commercial Distribution 🇺🇸 United States

HAcancellous™ PEEK-C

DI: M711591417070 · Model: 59-141707 · INNO Holdings, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
HAcancellous™ PEEK-C
Primary DI
M711591417070
Version / Model
59-141707
Company Name
INNO Holdings, Inc.
Labeler DUNS
141620464
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-29
Public Version
3
Public Version Date
2025-12-18
Public Version Status
Update
Public Device Record Key
5f816f73-405f-49c9-9866-7451bbe98c50
Distribution End Date
2025-12-04

Device Description

HAcancellous PEEK-C, 14L x 17W x 7H x 8°, HA PEEK, Ta

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Package M711591417071
Primary M711591417070

Customer Contacts

Phone
801-261-2236

Device Sizes

Type Value Unit Text
Length 14 Millimeter
Height 7 Millimeter
Angle 8 degree
Width 17 Millimeter