FDA.reportPublic FDA data

ULTRA-DRIVE®

Primary DI
00880304372917
Brand
ULTRA-DRIVE®
Company
Biomet Orthopedics, LLC
Model
423833
Catalog number
423833
Published
2016-09-26
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
JDXINSTRUMENT, SURGICAL, SONIC AND ACCESSORY/ATTACHMENT

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
JDXInstrument, Surgical, Sonic And Accessory/AttachmentOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K031280000
K900003000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K031280000ULTRA-DRIVE 3Biomet, Inc.2003-09-22JDX
K900003000SYSTEM TEN MODEL 100 SURGICAL SYSTEMAdvanced Osseous Technologies1990-03-16JDX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00880304372917PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00880304372917008803043729178803043729170880304372917

GMDN Terms#

Term, Definition table
TermDefinition
Surgical power tool irrigation-control deviceA device designed to be activated by the surgeon to regulate the flow of irrigation fluid (normally sterile saline) to the surgical site where a rotational high-speed cutting tool [e.g., 40.000 - 90.000 revolutions per minute (rpm)] is being applied to bone; primarily to provide the fluid as a coolant to the cutting tool (e.g., a bur or drill bit) and the site to avoid necrosis. It typically consists of tubing, connectors, and a simple electrically or pneumatically activated valve in which the coolant tubing is placed and which is pinched to regulate the fluid flow. It is typically made of metal and/or synthetic materials. This is a reusable device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)348-9500customerservice@zimmerbiomet.com

Regulatory Flags#

DUNS number
129278169
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00887868561368VersaNail®2810-13-0372810130372023-09-07
00889024707061A.L.P.S.®2142-35-0072142350072026-05-11
00889024707078DRILL BIT2312002012312002012026-05-11
00889024707085DRILL BIT8290-29-0708290290702026-05-11
00880304410541FIBER OPTICS FOR RC RETRACTOR9085349085342019-06-11
00880304321946BIFURCATED FIBER OPTIC CABLE31-55550231-5555022017-07-28
008803044639124MM X 9FT. LIGHT CABLE9061179061172017-07-28
00889024707054CALIBRATED DRILL BIT2142-27-0702142270702026-04-27
00880304233102Biomet® Knee System1418721418722015-10-24
00880304233126Biomet® Knee System1418741418742015-10-24
00880304233140Biomet® Knee System1418761418762015-10-24
00880304233164Biomet® Knee System1418781418782015-10-24
00880304233171Biomet® Knee System1418801418802015-10-24
00880304233188Biomet® Knee System1418821418822015-10-24
00880304433403Vanguard® Knee System1841441841442015-10-24
00880304433410Vanguard® Knee System1841811841812015-10-24
00880304433564Vanguard® Knee System1842851842852015-10-24
00880304433984Vanguard® Knee System1842801842802015-10-24
00880304434356Vanguard® Knee System1842651842652015-10-24
00880304434363Vanguard® Knee System1842701842702015-10-24

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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E322036300090MECTRONMECTRON SPAJDX2026-04-20
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