FDA UDI Not in Commercial Distribution 🇺🇸 United States

Screw

DI: 07613327036220 · Model: 6302-3-020 · Howmedica Osteonics Corp.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Screw
Primary DI
07613327036220
Version / Model
6302-3-020
Catalog Number
6302-3-020
Company Name
Howmedica Osteonics Corp.
Labeler DUNS
058311945
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
6
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
4e4e615e-38c9-468c-87a7-60c4a57ab30c
Distribution End Date
2016-08-26

Device Description

Bone Screw - Hex Drive Selftap

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
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Primary 07613327036220

Premarket Submissions

Submission Number Supplement Number
K933102 000
K974685 000

Device Sizes

Type Value Unit Text
Length 20.0 Millimeter
Device Size Text, specify Diameter: 6.5 Millimeter