FDA UDI Not in Commercial Distribution 🇺🇸 United States

ENDOFIX

DI: 03596010390653 · Model: 7207479 · Smith & Nephew, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOFIX
Primary DI
03596010390653
Version / Model
7207479
Catalog Number
7207479
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-12
Public Version
7
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
1c6439fb-18b6-4b10-94aa-2275d8849146
Distribution End Date
2022-03-17

Device Description

SCR ENDO-FIX L 9X30 BIOABS. INTF

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
MAI FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE
HWC Screw, fixation, bone

GMDN Terms

Code Name
45039 Bioabsorbable orthopaedic bone screw

Identifiers

Type ID
Primary 03596010390653

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K984320 000