FDA UDI In Commercial Distribution 🇺🇸 United States

Excella II®

DI: M711PR55500 · Model: PR5550 · INNO Holdings, Inc.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Excella II®
Primary DI
M711PR55500
Version / Model
PR5550
Catalog Number
PR5550
Company Name
INNO Holdings, Inc.
Labeler DUNS
141620464
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-05
Public Version
4
Public Version Date
2026-02-05
Public Version Status
Update
Public Device Record Key
7ffaaf5b-2995-43d0-a6d1-cf7dbfb08300

Device Description

Ti 6Al 4V (ELI)

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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWQ Appliance, Fixation, Spinal Intervertebral Body
KWP Appliance, Fixation, Spinal Interlaminal
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease

GMDN Terms

Code Name
65116 Bone-screw internal spinal fixation system rod

Identifiers

Type ID
Primary M711PR55500

Customer Contacts

Phone
801-261-2236

Device Sizes

Type Value Unit Text
Length 50 Millimeter
Outer Diameter 5.5 Millimeter