FDA UDI In Commercial Distribution 🇺🇸 United States

Blustone Synergy Lumbar TLIF Inserter/Pusher (Obsidian)

DI: 00810482031382 · Model: 9100-TI01 · BLUSTONE SYNERGY, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Blustone Synergy Lumbar TLIF Inserter/Pusher (Obsidian)
Primary DI
00810482031382
Version / Model
9100-TI01
Company Name
BLUSTONE SYNERGY, LLC
Labeler DUNS
033467608
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-29
Public Version
5
Public Version Date
2019-04-23
Public Version Status
Update
Public Device Record Key
c3213c5f-e825-4600-8c0e-96a9d96b3829

Device Description

The BluStone Synergy Obsidian System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The Obsidian TLIF implant inserter/pusher is designed to allow for disassembly during cleaning and sterilization. Instructions regarding disassembly, cleaning and sterilization of the inserter/pusher instrument are provided in the product insert.

Device Characteristics

Single Use
No
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
No
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FZX Guide, Surgical, Instrument

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00810482031382

Customer Contacts

Phone
800-232-9108

Device Sizes

Type Value Unit Text
Device Size Text, specify 45° X .05 Chamfer
Lumen/Inner Diameter 0.218 Inch