FDA UDI In Commercial Distribution 🇺🇸 United States

Freedom

DI: 00811767026673 · Model: MLCRXD310-K · MAXX ORTHOPEDICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Freedom
Primary DI
00811767026673
Version / Model
MLCRXD310-K
Company Name
MAXX ORTHOPEDICS, INC.
Labeler DUNS
792030103
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
8babae13-2d00-4179-86f2-3fdb8a380cb8

Device Description

Tibial Articular Surface CR, Size D3-4, 10mm

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
46585 Tibial insert

Identifiers

Type ID
Primary 00811767026673

Premarket Submissions

Submission Number Supplement Number
K091280 000