FDA UDI In Commercial Distribution 🇺🇸 United States

Mergence™-S

DI: 00889024316201 · Model: 96-101-01091 · ZIMMER TRABECULAR METAL TECHNOLOGY INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Mergence™-S
Primary DI
00889024316201
Version / Model
96-101-01091
Catalog Number
96-101-01091
Company Name
ZIMMER TRABECULAR METAL TECHNOLOGY INC.
Labeler DUNS
793120965
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-20
Public Version
5
Public Version Date
2020-06-18
Public Version Status
Update
Public Device Record Key
d6315ae8-2059-4915-942c-5e7c68f17607

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
HXB PROBE
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 00889024316201

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K103033 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Size: 11 x 11 mm
Height 9 Millimeter