FDA UDI In Commercial Distribution 🇺🇸 United States

ACDF Stand Alone Cervical

DI: 07630040725910 · Model: 03.18.221 · Medacta International SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACDF Stand Alone Cervical
Primary DI
07630040725910
Version / Model
03.18.221
Company Name
Medacta International SA
Labeler DUNS
488227125
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-26
Public Version
1
Public Version Date
2020-07-06
Public Version Status
New
Public Device Record Key
e40b4a6c-664f-47d8-9920-8f4a2ea5544a

Device Description

Mecta-C SA – Plate Flush Lag h11

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 07630040725910

Premarket Submissions

Submission Number Supplement Number
K192906 000