FDA UDI In Commercial Distribution 🇺🇸 United States

ACIS

DI: 10705034763002 · Model: 08.843.812S · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ACIS
Primary DI
10705034763002
Version / Model
08.843.812S
Catalog Number
08843812S
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
4
Public Version Date
2020-09-02
Public Version Status
Update
Public Device Record Key
d6468f7a-fa6f-4c7e-a442-ba3fb90682d7

Device Description

ACIS IMPLANT-STERILE CONVEX/SMALL-12MM HEIGHT

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Secondary H98108843812S0
Primary 10705034763002

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K120275 000