FDA UDI In Commercial Distribution 🇺🇸 United States

BIOMET KNEE SYSTEM

DI: 00880304002913 · Model: 141512 · Biomet Orthopedics, LLC
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BIOMET KNEE SYSTEM
Primary DI
00880304002913
Version / Model
141512
Catalog Number
141512
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
4
Public Version Date
2019-12-11
Public Version Status
Update
Public Device Record Key
9b143a16-1590-4bf8-ba28-9c7ad5863e34

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MBH PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
MBV Prosthesis, knee, patello/femorotibial, semi-constrained, uhmwpe, pegged, cemented, polymer/metal/polymer
HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER
OIY Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive

GMDN Terms

Code Name
32832 Uncoated knee tibia prosthesis, metallic

Identifiers

Type ID
Primary 00880304002913

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K010212 000
K142933 000
K171054 000
K915132 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 67 MM