FDA UDI In Commercial Distribution 🇺🇸 United States

Comprehensive Modular Hybrid Glenoid

DI: 00880304992818 · Model: SSI000916 · Biomet Orthopedics, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Comprehensive Modular Hybrid Glenoid
Primary DI
00880304992818
Version / Model
SSI000916
Catalog Number
SSI000916
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-19
Public Version
4
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
c826005a-c40a-45ef-8fc6-9cbd74665f3f

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
KWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

GMDN Terms

Code Name
58784 Humeral head prosthesis trial, reusable

Identifiers

Type ID
Primary 00880304992818

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K060694 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Small