FDA UDI In Commercial Distribution 🇺🇸 United States

Dynagraft II Putty

DI: 10889981055554 · Model: 02-2010-025 · ISOTIS ORTHOBIOLOGICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Dynagraft II Putty
Primary DI
10889981055554
Version / Model
02-2010-025
Catalog Number
02-2010-025
Company Name
ISOTIS ORTHOBIOLOGICS, INC.
Labeler DUNS
801089152
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
aea46482-e6ec-421b-8ffd-c8f74c82808f

Device Description

DynaGraft II Putty, 2.5cc - derived from selected donated human bone tissue that has been processed into particles. The bone particles are subsequently demineralized using a hydrochloric acid process. The demineralized bone matrix (DBM) is combined with an inert reverse phase carrier and formulated to a gel or putty-like consistency.

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
Yes
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
MQV FILLER, BONE VOID, CALCIUM COMPOUND

GMDN Terms

Code Name
47257 Bone matrix implant, human-derived

Identifiers

Type ID
Secondary M3860220100251
Primary 10889981055554

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K040419 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 2.5cc

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius