FDA UDI In Commercial Distribution 🇺🇸 United States

Vitoss BA Injectable

DI: 07613327064797 · Model: 2102-2305 · Stryker Orthobiologics
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vitoss BA Injectable
Primary DI
07613327064797
Version / Model
2102-2305
Catalog Number
2102-2305
Company Name
Stryker Orthobiologics
Labeler DUNS
849227939
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-12
Public Version
4
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
354abb18-b89a-4a4c-9ec3-bcae24360f7c

Device Description

Bone graft substitute

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
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MQV FILLER, BONE VOID, CALCIUM COMPOUND

GMDN Terms

Code Name
17751 Bone matrix implant, synthetic, non-antimicrobial

Identifiers

Type ID
Primary 07613327064797

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K163621 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Total Volume: 5.0 Cubic Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 30 Degrees Celsius