FDA UDI Not in Commercial Distribution 🇺🇸 United States

POLARCUPTM

DI: 07611996096255 · Model: 75017202 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
POLARCUPTM
Primary DI
07611996096255
Version / Model
75017202
Catalog Number
75017202
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-29
Public Version
7
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
15737f80-dd2a-406a-af3e-9ca272eb8914
Distribution End Date
2022-03-17

Device Description

POLARCUP SHELL 59 CEMENTED

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
KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented

GMDN Terms

Code Name
43167 Acetabular shell

Identifiers

Type ID
Primary 07611996096255

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K070278 000