FDA UDI In Commercial Distribution 🇺🇸 United States

POLARCUP

DI: 07611996118353 · Model: 75100444 · Smith & Nephew, Inc.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
POLARCUP
Primary DI
07611996118353
Version / Model
75100444
Catalog Number
75100444
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-25
Public Version
7
Public Version Date
2025-08-13
Public Version Status
Update
Public Device Record Key
212cace2-cb18-4660-b66b-9636b1c8abeb

Device Description

POLARCUP SHELL TI-PLASMA/HA 59 NON-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
MR Conditional
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
LWJ Prosthesis, hip, semi-constrained, metal/polymer, uncemented
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented

GMDN Terms

Code Name
43167 Acetabular shell

Identifiers

Type ID
Primary 07611996118353

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K122244 000
K211176 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
: -