FDA UDI In Commercial Distribution 🇺🇸 United States

C2 Hip

DI: 08033390071666 · Model: 9045.16.013 · LIMACORPORATE SPA
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
C2 Hip
Primary DI
08033390071666
Version / Model
9045.16.013
Catalog Number
9045.16.013
Company Name
LIMACORPORATE SPA
Labeler DUNS
432066322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-13
Public Version
5
Public Version Date
2019-07-05
Public Version Status
Update
Public Device Record Key
8a141470-c4df-4b2e-b58e-bc75b78140a8

Device Description

C2 Hip - Lateralized Trial Neck

Device Characteristics

Single Use
No
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
Yes
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
LWJ Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented

GMDN Terms

Code Name
58481 Femoral stem prosthesis trial

Identifiers

Type ID
Primary 08033390071666

Premarket Submissions

Submission Number Supplement Number
K170473 000