FDA UDI In Commercial Distribution 🇺🇸 United States

Zero-P VA

DI: 10705034720593 · Model: 03.647.782 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Zero-P VA
Primary DI
10705034720593
Version / Model
03.647.782
Catalog Number
03647782
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
5
Public Version Date
2022-06-01
Public Version Status
Update
Public Device Record Key
a7f8a03a-7c5c-4690-8d2a-637efb86cc37

Device Description

ZERO-P VA TRIAL SPACER W/STOP CONVEX/12MM HEIGHT

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
OVE Intervertebral fusion device with integrated fixation, cervical

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Secondary H981036477820
Primary 10705034720593
Direct Marking 07611819404274

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K112068 000