FDA.reportPublic FDA data

PRECICE® Trauma Nail System

Primary DI
00812258027100
Brand
PRECICE® Trauma Nail System
Company
NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
Model
FXR1-000
Catalog number
FXR1-000
Device description
Fracture Reducer
Published
2017-11-03
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
HWNInstrument, Compression

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HWNInstrument, CompressionOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00812258027100PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00812258027100008122580271008122580271000812258027100

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic bone-reduction toolA hand-held manual surgical instrument that is fed down the intramedullary canal of a long bone (e.g., the femur) to help reposition a fracture where the two sections are out of alignment to achieve reduction for consequent reaming and nailing of the bone. It is typically a short cylindrical device with a protruding pointed tip (straight or angled) and which is secured to the distal end of a long, thin, flexible rod/shaft having a handle at the proximal end. It is pressed down the intramedullary canal to the fracture site and the surgeon manipulates the alignment, reducing the bone fragments under image-intensifier control. It is made of high-grade stainless steel. This is a reusable device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
855-435-5478csdepartment@nuvasive.com
866-456-2871info@globusmedical.com

Regulatory Flags#

DUNS number
837845234
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00195377024282Precice InstrumentOSR2-0002023-01-26
00195377066206Precice InstrumentSPAS-3.22023-01-26
00195377066305Precice Ankle Salvage SystemAST1-0002023-01-26
00195377066701Precice InstrumentSPT1-0002023-01-26
00195377066718Precice InstrumentSPR1-0002023-01-26
00812258028602Precice InstrumentSDG2-0002023-01-26
00887517001238Precice InstrumentOSG1-0002023-01-26
00887517001252Precice InstrumentOSG3-0002023-01-26
00887517001290Precice InstrumentCRT1-0002023-01-26
00887517001313Precice InstrumentOSP5-0752023-01-26
00887517001320Precice InstrumentOSP5-1002023-01-26
00887517054272Precice InstrumentsOTA1-0002023-01-26
00887517885234Precice InstrumentHCB3-0002023-01-26
00887517937148Precice InstrumentKWS1-0022023-01-26
00887517937155Precice InstrumentKWS2-0002023-01-26
00195377168276PRECICE ScrewsTSA5-100TSA5-1002017-10-09
00195377168283PRECICE ScrewsTSA5-095TSA5-0952017-10-09
00195377168290PRECICE ScrewsTSA5-080TSA5-0802017-10-09
00195377168603PRECICE ScrewsTSA5-070TSA5-0702017-10-09
00195377168610PRECICE ScrewsTSA5-060TSA5-0602017-10-09

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