FDA UDI In Commercial Distribution 🇺🇸 United States

SeaSpine Spacer System - Hollywood VI NanoMetalene

DI: 00889981064580 · Model: 34-9108-S · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SeaSpine Spacer System - Hollywood VI NanoMetalene
Primary DI
00889981064580
Version / Model
34-9108-S
Catalog Number
34-9108-S
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-02
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
0164d16f-7237-4d5a-b6e5-bbfc44259d2b

Device Description

Hollywood VI NM Sterile 11mm x 30mm x 8mm, Lordotic

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
MAX Intervertebral fusion device with bone graft, lumbar
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary 00889981064580

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K162715 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 11mm x 30mm x 8mm