FDA UDI In Commercial Distribution 🇺🇸 United States

Movement®

DI: 10381780236900 · Model: TRL89030MT · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Movement®
Primary DI
10381780236900
Version / Model
TRL89030MT
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-15
Public Version
5
Public Version Date
2023-01-25
Public Version Status
Update
Public Device Record Key
b9d5b040-fff1-4211-b086-dba101569bbb
Distribution End Date
2026-12-31

Device Description

The Metatarsal Trial is used to evaluate the size and fit of the implant.

Device Characteristics

Single Use
No
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
KWD PROSTHESIS, TOE, HEMI-, PHALANGEAL

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Secondary M269TRL89030MT1
Primary 10381780236900

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K092047 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Size 30; .709 in L