FDA UDI In Commercial Distribution 🇺🇸 United States

Ti Cancellous Screw

DI: 04712771504736 · Model: 5206-1035 · UNITED ORTHOPEDIC CORP.
Product Codes
4
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ti Cancellous Screw
Primary DI
04712771504736
Version / Model
5206-1035
Catalog Number
5206-1035
Company Name
UNITED ORTHOPEDIC CORP.
Labeler DUNS
656700556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
4
Public Version Date
2018-08-07
Public Version Status
Update
Public Device Record Key
3c4007fc-2b05-4a59-ad8d-29b32d611b3b

Device Description

Ti Cancellous Screw, Ø6.5 x 35mm

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

GMDN Terms

Code Name
34204 Ceramic-on-ceramic total hip prosthesis
33715 Ceramic-on-polyethylene total hip prosthesis

Identifiers

Type ID
Primary 04712771504736

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K122185 000

Device Sizes

Type Value Unit Text
Length 35 Millimeter
Device Size Text, specify Ø6.5