FDA.reportPublic FDA data

PRECICE® Trauma Nail System

Primary DI
00812258027605
Brand
PRECICE® Trauma Nail System
Company
NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
Model
CDT12.5-30T360
Catalog number
CDT12.5-30T360
Device description
Orthopedic trauma intramedullary rod, antegrade tibia 10° bend, 12.5 mm diameter, 360 mm length
Published
2017-10-02
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HSBRod, Fixation, Intramedullary And Accessories

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HSBRod, Fixation, Intramedullary And AccessoriesOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K162927000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K162927000PRECICE UNYTE CoCr SystemNuvasive Specialized Orthopedics, Inc.2017-04-06HSB

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00812258027605PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00812258027605008122580276058122580276050812258027605

GMDN Terms#

Term, Definition table
TermDefinition
Tibia nail, sterileA sterile rod made of metal or other material which, when inserted into the intramedullary canal of the tibia, acts to immobilize by holding the ends of a fractured bone in position to promote healing. The device may also be used to support the bone in the presence of a pathological condition, or for knee arthrodesis. The device may be a locked or unlocked model, and possess components to assist fixation of more proximal or distal conditions. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Outer Diameter12.5Millimeter

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
855-435-5477csdepartment@nuvasive.com
866-456-2871info@globusmedical.com

Regulatory Flags#

DUNS number
837845234
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00195377108555PRECICETPT6-110-B-S2023-10-04
00195377108562PRECICETPT6-105-B-S2023-10-04
00195377108579PRECICETPT6-100-B-S2023-10-04
00195377108586PRECICETPT6-950-B-S2023-10-04
00195377108593PRECICETPT6-900-B-S2023-10-04
00195377108609PRECICETPT6-850-B-S2023-10-04
00195377108623PRECICETPT6-750-B-S2023-10-04
00195377108630PRECICETPT6-700-B-S2023-10-04
00195377108647PRECICETPT6-650-B-S2023-10-04
00195377108654PRECICETPT6-600-B-S2023-10-04
00195377108661PRECICETPT6-110-A-S2023-10-04
00195377108678PRECICETPT6-105-A-S2023-10-04
00195377108685PRECICETPT6-100-A-S2023-10-04
00195377108692PRECICETPT6-950-A-S2023-10-04
00195377108708PRECICETPT6-900-A-S2023-10-04
00195377108715PRECICETPT6-850-A-S2023-10-04
00195377108722PRECICETPT6-800-A-S2023-10-04
00195377108739PRECICETPT6-750-A-S2023-10-04
00195377108746PRECICETPT6-700-A-S2023-10-04
00195377108753PRECICETPT6-650-A-S2023-10-04

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Primary DI, Brand, Company table
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00888867417281Arthrex®ARTHREX, INC.HSB2026-07-22
00888867417298Arthrex®ARTHREX, INC.HSB2026-07-22
00888867417304Arthrex®ARTHREX, INC.HSB2026-07-22
00888867417311Arthrex®ARTHREX, INC.HSB2026-07-22
00888867417328Arthrex®ARTHREX, INC.HSB2026-07-22
00888867417335Arthrex®ARTHREX, INC.HSB2026-07-22
00888867417342Arthrex®ARTHREX, INC.HSB2026-07-22
00888867417359Arthrex®ARTHREX, INC.HSB2026-07-22
00888867417366Arthrex®ARTHREX, INC.HSB2026-07-22
00888867417373Arthrex®ARTHREX, INC.HSB2026-07-22
00888867417380Arthrex®ARTHREX, INC.HSB2026-07-22
00888867417397Arthrex®ARTHREX, INC.HSB2026-07-22
00888867417403Arthrex®ARTHREX, INC.HSB2026-07-22
00888867417410Arthrex®ARTHREX, INC.HSB2026-07-22
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00193982660260AUTOBAHNGLOBUS MEDICAL, INC.HSB2026-06-10
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00193982660307AUTOBAHNGLOBUS MEDICAL, INC.HSB2026-06-10