FDA UDI In Commercial Distribution 🇺🇸 United States

SYMPHONY

DI: 10705034520155 · Model: 1020-23-102S · Medos International Sàrl
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SYMPHONY
Primary DI
10705034520155
Version / Model
1020-23-102S
Catalog Number
102023102S
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
697ea81a-6a5f-4cba-9b43-f931a0faedca

Device Description

SYMPHONY OCT SYSTEM CROSSCONNECTOR HEAD TO HEAD 30 to 42mm

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKG Posterior cervical screw system

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 10705034520155

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K181949 000
K190895 000