FDA UDI In Commercial Distribution 🇺🇸 United States

Synergy Disc Instruments

DI: M67091000009560 · Model: 910-00009-56 · Synergy Spine Solutions Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Synergy Disc Instruments
Primary DI
M67091000009560
Version / Model
910-00009-56
Catalog Number
910-00009-56
Company Name
Synergy Spine Solutions Inc
Labeler DUNS
144962703
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-17
Public Version
1
Public Version Date
2026-04-27
Public Version Status
New
Public Device Record Key
94ece922-0dfe-480a-8b44-89d2f098af70

Device Description

Trial, Large, 6mm, 0°

Device Characteristics

Single Use
No
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
QLQ Manual Instruments Designed For Use With Total Disc Replacement Devices

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary M67091000009560

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K253392 000

Device Sizes

Type Value Unit Text
Angle 0 degree
Height 6 Millimeter