FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® BioMotion® Cannulated Hemi System

DI: 10381780116356 · Model: HM1500 · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® BioMotion® Cannulated Hemi System
Primary DI
10381780116356
Version / Model
HM1500
Catalog Number
HM1500
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
5
Public Version Date
2023-01-25
Public Version Status
Update
Public Device Record Key
33dc1fa4-b13e-49b6-9bf9-70fe1d90e438
Distribution End Date
2026-12-31

Device Description

The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioMotion® Cannulated Hemi System as a partial joint replacement for the first metatarsophalangeal joint (MPJ). The Cannulated Implants are made from Titanium Alloy (ASTM F-136).

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
KWD PROSTHESIS, TOE, HEMI-, PHALANGEAL

GMDN Terms

Code Name
33700 Total metatarsophalangeal joint prosthesis, one-piece

Identifiers

Type ID
Primary 10381780116356
Secondary M268HM15001

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K083469 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 12.05 mm L x 15 mm W x 10.8 mm H