FDA UDI In Commercial Distribution 🇺🇸 United States

SYMPHONY

DI: 10705034513751 · Model: 1020-35-740 · Medos International Sàrl
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SYMPHONY
Primary DI
10705034513751
Version / Model
1020-35-740
Catalog Number
102035740
Company Name
Medos International Sàrl
Labeler DUNS
482661753
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-08-02
Public Version
2
Public Version Date
2019-08-15
Public Version Status
Update
Public Device Record Key
b95395ba-825f-40c1-a396-2fae5c9231c8

Device Description

SYMPHONY OCT SYSTEM SHAFT POLYAXIAL SCREW Diameter 4.0 Rod, 3.5X40mm

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
MR Conditional
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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKG Posterior cervical screw system

GMDN Terms

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

Identifiers

Type ID
Primary 10705034513751

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K181949 000
K190895 000