FDA UDI In Commercial Distribution 🇺🇸 United States

MAXIM VI KNEE SYSTEM

DI: 00880304206359 · Model: 11-144120 · Biomet Orthopedics, LLC
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MAXIM VI KNEE SYSTEM
Primary DI
00880304206359
Version / Model
11-144120
Catalog Number
11-144120
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
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
1ddd1eb7-c3d5-4aa9-af6a-4a66d095cc66

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

GMDN Terms

Code Name
46585 Tibial insert

Identifiers

Type ID
Primary 00880304206359

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K171054 000
K921182 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 20MM 79MM