FDA.reportPublic FDA data

NA

Primary DI
00889024432994
Brand
NA
Company
Zimmer, Inc.
Model
8011-20-20
Catalog number
00-8011-020-20
Published
2016-05-24
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
JDIProsthesis, hip, semi-constrained, metal/polymer, cemented
LZNCEMENT OBTURATOR

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
JDIProsthesis, Hip, Semi-Constrained, Metal/Polymer, CementedOrthopedic2
LZNCement ObturatorGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K001733000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K001733000ALLEN MEDULLARY CEMENT PLUGS, ZIMMER POLY PLUG INTRAMEDULLARY SYSTEM, MODEL 8011 SERIES & 1109 & 8109 SERIESZimmer, Inc.2000-06-20JDI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00889024432994PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00889024432994008890244329948890244329940889024432994

GMDN Terms#

Term, Definition table
TermDefinition
Polymer orthopaedic cement restrictor, non-bioabsorbable, sterileA sterile, 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 is not intended for spinal indication.

Device Sizes#

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

Sterilization Methods#

Method table
Method

Contacts#

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

Regulatory Flags#

DUNS number
056038268
Device count
1
Lot or batch
true
Expiration date on label
true
Contains natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00889024701281Identity® Shoulder System11007733110077332026-06-10
00889024701298Identity® Shoulder System11007734110077342026-06-10
00889024701304Identity® Shoulder System11007735110077352026-06-10
00889024701311Identity® Shoulder System11007736110077362026-06-10
00889024701328Identity® Shoulder System11007737110077372026-06-10
00889024701335Identity® Shoulder System11007738110077382026-06-10
00889024701342Identity® Shoulder System11007739110077392026-06-10
00889024701359Identity® Shoulder System11007740110077402026-06-10
00889024701366Identity® Shoulder System11007741110077412026-06-10
00889024701373Identity® Shoulder System11007742110077422026-06-10
00889024701380Identity® Shoulder System11007743110077432026-06-10
00889024701397Identity® Shoulder System11007744110077442026-06-10
00889024701403Identity® Shoulder System11007745110077452026-06-10
00889024701410Identity® Shoulder System11007746110077462026-06-10
00889024701427Identity® Shoulder System11007747110077472026-06-10
00889024701434Identity® Shoulder System11007748110077482026-06-10
00889024701441Identity® Shoulder System11007749110077492026-06-10
00889024701458Identity® Shoulder System11007750110077502026-06-10
00889024701465Identity® Shoulder System11007751110077512026-06-10
00889024701472Identity® Shoulder System11007752110077522026-06-10

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Primary DI, Brand, Company table
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00810068850086Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
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00810068850109Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
00810068850123Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
00810068850130Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
00810068850147Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
00810068850154Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
00810068850185Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
00810068850192Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
00810068850208Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
00810068850215Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
00810068850222Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
00810068850239Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
00810068850246Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
00810068850284Biocore9 Acetabular Bearing SystemBiocore9, LLCJDI2026-06-26
00810068850307Biocore9 Acetabular Bearing SystemBiocore9, LLCJDI2026-06-26
00810068850321Biocore9 Acetabular Bearing SystemBiocore9, LLCJDI2026-06-26
00810068850338Biocore9 Acetabular Bearing SystemBiocore9, LLCJDI2026-06-26
00810068850345Biocore9 Acetabular Bearing SystemBiocore9, LLCJDI2026-06-26
00810068850635Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
00810068850642Biocore9 Acetabular Cup SystemBiocore9, LLCJDI2026-06-26
00810068850703Biocore9 Acetabular Bearing SystemBiocore9, LLCJDI2026-06-26
00810068850710Biocore9 Acetabular Bearing SystemBiocore9, LLCJDI2026-06-26
00810068850727Biocore9 Acetabular Bearing SystemBiocore9, LLCJDI2026-06-26
00810068850734Biocore9 Acetabular Bearing SystemBiocore9, LLCJDI2026-06-26
00810068850741Biocore9 Acetabular Bearing SystemBiocore9, LLCJDI2026-06-26
00810068850758Biocore9 Acetabular Bearing SystemBiocore9, LLCJDI2026-06-26
00810068850772Biocore9 Acetabular Bearing SystemBiocore9, LLCJDI2026-06-26
00810068850895Biocore9 Acetabular Bearing SystemBiocore9, LLCJDI2026-06-26