FDA UDI In Commercial Distribution 🇺🇸 United States

OsteoTorrent

DI: 10889981284039 · Model: 57000012 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OsteoTorrent
Primary DI
10889981284039
Version / Model
57000012
Catalog Number
57000012
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-16
Public Version
1
Public Version Date
2022-02-24
Public Version Status
New
Public Device Record Key
723f2d65-0319-468d-98df-12cb55c367c8

Device Description

OsteoTorrent™, Dry DBM Putty with Accell, 1.25cc

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
Primary 10889981284039

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K212135 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius