FDA UDI In Commercial Distribution 🇺🇸 United States

SynFix-LR

DI: 10705034752990 · Model: 04.802.212 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SynFix-LR
Primary DI
10705034752990
Version / Model
04.802.212
Catalog Number
04802212
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
bc61a4ac-9619-4066-85dc-68adb66ab4dd

Device Description

4.0MM TI LOCKING SCREW-FINE TIP 25MM FOR SYNFIX-LR

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
OVD Intervertebral fusion device with integrated fixation, lumbar

GMDN Terms

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

Identifiers

Type ID
Secondary H981048022120
Primary 10705034752990

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K072253 000