Blustone Synergy Spinal Intervertebral Body Fixation System (Silica) - The Silica implants are rectangular shaped blocks - BLUSTONE SYNERGY, LLC

Duns Number:033467608

Device Description: The Silica implants are rectangular shaped blocks in parallel, 3° and 6° lordotic configur The Silica implants are rectangular shaped blocks in parallel, 3° and 6° lordotic configurations of various heights. The implants are designed with a 15mm x 13mm footprint in heights ranging from 20 to 50mm in three (3) mm increments. The device is hollow to allow for placement of autograft and/or allogenic bone graft and facilitate fusion, and contains tantalum markers to assist the surgeon with proper placement of the device. The device may be implanted as a single device via an anterior approach.

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More Product Details

Catalog Number

-

Brand Name

Blustone Synergy Spinal Intervertebral Body Fixation System (Silica)

Version/Model Number

1513-C320

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K172330

Product Code Details

Product Code

MQP

Product Code Name

Spinal Vertebral Body Replacement Device

Device Record Status

Public Device Record Key

e5ad3a1e-84fa-46f5-934e-618a18ca0433

Public Version Date

February 24, 2020

Public Version Number

4

DI Record Publish Date

January 29, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"BLUSTONE SYNERGY, LLC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 76
2 A medical device with a moderate to high risk that requires special controls. 64