FDA UDI Not in Commercial Distribution 🇺🇸 United States

KANEDA SR

DI: 10705034243290 · Model: 52102835MB · DEPUY SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KANEDA SR
Primary DI
10705034243290
Version / Model
52102835MB
Catalog Number
52102835MB
Company Name
DEPUY SPINE, LLC
Labeler DUNS
107105876
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
5
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
0f99b7cb-ce9b-43d2-8546-45ec6dddecf1
Distribution End Date
2018-06-20

Device Description

KANEDA SR ANTERIOR SYSTEM BLUNT TIP CLOSED SCREW 6.35 x 6.25 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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 10705034243290

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K943819 000