FDA UDI In Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780237235 · Model: SHP9004820 · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra®
Primary DI
10381780237235
Version / Model
SHP9004820
Catalog Number
SHP-900-48/20
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
9658a0b6-0ec0-4182-b544-5368b184f470
Distribution End Date
2026-12-31

Device Description

Humeral Resurfacing Arthroplasty

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
HSD PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED

GMDN Terms

Code Name
10455 Bone cutter

Identifiers

Type ID
Secondary M269SHP90048201
Primary 10381780237235

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K062861 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Size 48/20