Fusion™ Lateral Instrument Set - RASP, LARGE, STRAIGHT - Pioneer Surgical Technology, Inc.

Duns Number:793384496

Device Description: RASP, LARGE, STRAIGHT

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

38-RASP-LG-S

Brand Name

Fusion™ Lateral Instrument Set

Version/Model Number

38-RASP-LG-S

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

-

Product Code Details

Product Code

HTR

Product Code Name

RASP

Device Record Status

Public Device Record Key

905ec0b1-2247-4d3d-9332-5e5d481065fe

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

September 30, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"PIONEER SURGICAL TECHNOLOGY, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 3116
2 A medical device with a moderate to high risk that requires special controls. 5221