FDA UDI In Commercial Distribution 🇺🇸 United States

Paxeon Remedy

DI: 08177570201068 · Model: PR111-19-0500 · PAXEON RECONSTRUCTION LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Paxeon Remedy
Primary DI
08177570201068
Version / Model
PR111-19-0500
Company Name
PAXEON RECONSTRUCTION LLC
Labeler DUNS
080437990
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-14
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
717de67f-241b-414d-976e-b0288194a5d5

Device Description

Remedy Stem Size 5 Standard Offset

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
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

GMDN Terms

Code Name
33581 Coated hip femur prosthesis, modular

Identifiers

Type ID
Primary 08177570201068

Premarket Submissions

Submission Number Supplement Number
K133370 000