FDA.reportPublic FDA data

Quik-Use®

Primary DI
00889024376632
Brand
Quik-Use®
Company
Zimmer, Inc.
Model
5049-55
Published
2016-02-29
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
HTFCURETTE

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HTFCuretteGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00889024379756PackageGS18In Commercial Distribution
00889024376632PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00889024379756008890243797568890243797560889024379756
00889024376632008890243766328890243766320889024376632

GMDN Terms#

Term, Definition table
TermDefinition
Polymer orthopaedic cement restrictor, non-bioabsorbableA non-bioabsorbable, implantable device designed to be inserted into the medullary canal of a bone (e.g., femur, tibia, or humerus) during orthopaedic surgery to prevent cement progression in the diaphysis and therefore facilitate cement pressurization during the introduction of an implant. It is typically made of polyetheretherketone (PEEK) or ultrahigh molecular weight polyethylene (UHMWPE) and is available in a variety of designs (e.g., straight or tapered, hollow with a fenestrated surface), and it may have a toothed surface to prevent its migration from the desired location. It may incorporate a metal orientation marker for radiographs and it is not intended for spinal application.

Contacts#

Phone, Email table
PhoneEmail
+1(800)348-2759zimmer.consumerrelations@zimmer.com

Regulatory Flags#

DUNS number
056038268
Device count
1
Premarket exempt
true
Kit
true
Lot or batch
true
Contains natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00889024702356OsseoFit00-5381-017-1100-5381-017-112026-10-28
00889024702363OsseoFit00-5381-017-1200-5381-017-122026-10-28
00889024702370OsseoFit00-5381-017-1300-5381-017-132026-10-28
00889024702387OsseoFit00-5381-017-1400-5381-017-142026-10-28
00889024702394OsseoFit00-5381-017-1500-5381-017-152026-10-28
00889024702400OsseoFit00-5381-017-1600-5381-017-162026-10-28
00889024702417OsseoFit00-5381-017-2100-5381-017-212026-10-28
00889024702424OsseoFit00-5381-017-2200-5381-017-222026-10-28
00889024702431OsseoFit00-5381-017-2300-5381-017-232026-10-28
00889024702448OsseoFit00-5381-017-2400-5381-017-242026-10-28
00889024702455OsseoFit00-5381-017-2500-5381-017-252026-10-28
00889024702462OsseoFit00-5381-017-2600-5381-017-262026-10-28
00889024702233OsseoFit00-5381-008-0500-5381-008-052026-10-27
00889024702240OsseoFit00-5381-008-0600-5381-008-062026-10-27
00889024702257OsseoFit00-5381-013-0000-5381-013-002026-10-27
00889024702264OsseoFit00-5381-013-1000-5381-013-102026-10-27
00889024702271OsseoFit00-5381-013-1100-5381-013-112026-10-27
00889024702295OsseoFit00-5381-013-1300-5381-013-132026-10-27
00889024702301OsseoFit00-5381-014-0000-5381-014-002026-10-27
00889024702318OsseoFit00-5381-014-0100-5381-014-012026-10-27

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00190776437084MillenniumAvalign Technologies, Inc.HTF2026-10-26
00190776437091MillenniumAvalign Technologies, Inc.HTF2026-10-26
00190776437107MillenniumAvalign Technologies, Inc.HTF2026-10-26
00190776437114MillenniumAvalign Technologies, Inc.HTF2026-10-26
00190776437121MillenniumAvalign Technologies, Inc.HTF2026-10-26
00190776437138MillenniumAvalign Technologies, Inc.HTF2026-10-26
00190776434151MillenniumAvalign Technologies, Inc.HTF2026-10-09
00190776433772MillenniumAvalign Technologies, Inc.HTF2026-10-08
00190776433321MillenniumAvalign Technologies, Inc.HTF2026-10-05
10705034579689N/AMedos International SàrlHTF2026-09-26
10705034579696N/AMedos International SàrlHTF2026-09-26
10705034579702N/AMedos International SàrlHTF2026-09-26
00810238290070PRINCETONPrinceton Medical Group, Inc.HTF2026-09-22
00850088713763PRINCETONPrinceton Medical Group, Inc.HTF2026-09-22
10705034579313N/AMedos International SàrlHTF2026-08-26
10705034579320N/AMedos International SàrlHTF2026-08-26
00850088713589PRINCETONPrinceton Medical Group, Inc.HTF2026-08-25
00190776419646MillenniumAvalign Technologies, Inc.HTF2026-08-23
00190776419653MillenniumAvalign Technologies, Inc.HTF2026-08-23
00190776426408MillenniumAvalign Technologies, Inc.HTF2026-08-18
00850088713435PRINCETONPrinceton Medical Group, Inc.HTF2026-08-14
00850088713442PRINCETONPrinceton Medical Group, Inc.HTF2026-08-14
00190776422240MillenniumAvalign Technologies, Inc.HTF2026-07-31
00190776422400MillenniumAvalign Technologies, Inc.HTF2026-07-31
00190776422417MillenniumAvalign Technologies, Inc.HTF2026-07-31
00190776422424MillenniumAvalign Technologies, Inc.HTF2026-07-31
00190776422509MillenniumAvalign Technologies, Inc.HTF2026-07-31
00190776422592MillenniumAvalign Technologies, Inc.HTF2026-07-31
00810168190464NAPACIFIC INSTRUMENTS, INC.HTF2026-07-06
B803PS0099100A0ORTHOMEDORTHO-MED, INC.HTF2026-06-26