FDA UDI In Commercial Distribution 🇺🇸 United States

MRS

DI: 07613327049367 · Model: 6485-3-015 · Howmedica Osteonics Corp.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MRS
Primary DI
07613327049367
Version / Model
6485-3-015
Catalog Number
6485-3-015
Company Name
Howmedica Osteonics Corp.
Labeler DUNS
058311945
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
88787c71-2bc3-4d5f-96f0-78f21ff68f95

Device Description

Straight Cemented Stem

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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KRO PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

GMDN Terms

Code Name
34191 Coated femoral stem prosthesis, modular

Identifiers

Type ID
Primary 07613327049367

Premarket Submissions

Submission Number Supplement Number
K040749 000
K965164 000

Device Sizes

Type Value Unit Text
Length 127.0 Millimeter
Device Size Text, specify Diameter: 15.0 Millimeter