FDA UDI Not in Commercial Distribution 🇺🇸 United States

Integra® TruArch®

DI: 10381780074342 · Model: TRUARCHIMP · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® TruArch®
Primary DI
10381780074342
Version / Model
TRUARCHIMP
Catalog Number
TRUARCHIMP
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-22
Public Version
6
Public Version Date
2023-05-02
Public Version Status
Update
Public Device Record Key
a42acb4c-2758-4574-b964-226d2bcca2b7
Distribution End Date
2023-03-31

Device Description

The Integra TruArch subtalar implant is a one-piece titanium implant for treating hyperpronation of the foot. It is designed to block forward, downward and medial displacement of the talus, thus allowing normal subtalar joint motion but blocking excessive pronation and the resulting sequela. The implant is offered in 5 sizes ranging from 8mm to 12mm in diameter. The system includes instruments to facilitate the placement of the implants.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Lot/Batch Number
No
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

GMDN Terms

Code Name
40352 Subtalar implant, non-bioabsorbable

Identifiers

Type ID
Secondary M268TRUARCHIMP1
Primary 10381780074342

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K111265 000