FDA UDI In Commercial Distribution 🇺🇸 United States

OsteoSurge 300 Putty

DI: 10889981055844 · Model: 56500050 · ISOTIS ORTHOBIOLOGICS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
OsteoSurge 300 Putty
Primary DI
10889981055844
Version / Model
56500050
Catalog Number
56500050
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
d5a93a45-0c79-42e4-8a5b-fd0c013c56da

Device Description

OsteoSurge300 Putty,5 cc - demineralized human bone mixed with poloxamer resorbable reverse phase medium. OsteoSurge300 is formulated into a putty form and is provided in a sterile, single use package.

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
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
Secondary M386565000501
Primary 10889981055844

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K061880 000
K103742 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 5cc

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius