FDA UDI In Commercial Distribution 🇺🇸 United States

Ballast™

DI: 10889981189259 · Model: 02-8000-160 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ballast™
Primary DI
10889981189259
Version / Model
02-8000-160
Catalog Number
02-8000-160
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-29
Public Version
1
Public Version Date
2023-09-06
Public Version Status
New
Public Device Record Key
0e67f0f3-1ecd-48f4-a8a0-c3f2b6c2b248

Device Description

Ballast, 115 x11mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
Yes
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
Yes
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
MBP Filler, bone void, osteoinduction (w/o human growth factor)
MQV FILLER, BONE VOID, CALCIUM COMPOUND

GMDN Terms

Code Name
47257 Bone matrix implant, human-derived

Identifiers

Type ID
Primary 10889981189259

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K193040 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 25 Degrees Celsius