FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® Total Foot System

DI: 10381780119166 · Model: 2822120 · Ascension Orthopedics, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Total Foot System
Primary DI
10381780119166
Version / Model
2822120
Catalog Number
2822120
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-09
Public Version
6
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
1875f832-7f36-4f54-9ffa-3ac0bd4e5560
Distribution End Date
2026-12-31

Device Description

The standard forefoot screw is used in the Integra Total Foot System. It is made from titanium and is a non-locking screw.

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
HWC Screw, fixation, bone
HRS PLATE, FIXATION, BONE

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 10381780119166
Secondary M26828221201

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K100502 000
K123000 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 20 mm L x 2.2 mm dia