FDA UDI In Commercial Distribution 🇺🇸 United States

Excella®

DI: M711EP40500 · Model: EP4050 · Innovasis, Inc.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Excella®
Primary DI
M711EP40500
Version / Model
EP4050
Catalog Number
EP4050
Company Name
Innovasis, Inc.
Labeler DUNS
156567492
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-17
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
ba2c1ed8-7305-4217-b72a-5b58817e50e4

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
Yes
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
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation
KWP Appliance, Fixation, Spinal Interlaminal
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary M711EP40500

Customer Contacts

Phone
801-261-2236

Premarket Submissions

Submission Number Supplement Number
K071921 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Length 40 -50mm