FDA UDI In Commercial Distribution 🇺🇸 United States

PRELUDE PATELLO-FEMORAL SYSTEM

DI: 00880304567238 · Model: 110004165 · Biomet Orthopedics, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PRELUDE PATELLO-FEMORAL SYSTEM
Primary DI
00880304567238
Version / Model
110004165
Catalog Number
110004165
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-28
Public Version
6
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
5b0a3b63-ea74-4434-ab64-6f03c7567ee9

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
Yes
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
KRR PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER

GMDN Terms

Code Name
45114 Bone-resection orthopaedic reamer, reusable

Identifiers

Type ID
Primary 00880304567238

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K143543 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 31MM STOP COLLAR