FDA.reportPublic FDA data

NA

Primary DI
00889024380189
Brand
NA
Company
Zimmer, Inc.
Model
8011-10-01
Published
2016-08-31
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
LZNCEMENT OBTURATOR

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
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
00889024380189PackageGS132In Commercial Distribution
00889024376724PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00889024380189008890243801898890243801890889024380189
00889024376724008890243767248890243767240889024376724

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@zimmer.com

Regulatory Flags#

DUNS number
056038268
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
true
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00889024081024XtraFix® Large External Fixation System00-5207-024-3000-5207-024-302016-08-09
00889024081055XtraFix® Large External Fixation System00-5207-032-3000-5207-032-302016-07-27
00889024081062XtraFix® Large External Fixation System00-5207-040-1000-5207-040-102016-07-28
00889024081079XtraFix® Large External Fixation System00-5207-040-7000-5207-040-702016-07-28
00889024081086XtraFix® Large External Fixation System00-5207-045-1000-5207-045-102016-07-28
00889024081093XtraFix® Large External Fixation System00-5210-009-0100-5210-009-012016-09-28
00889024081109XtraFix® Large External Fixation System00-5210-009-0200-5210-009-022016-09-28
00889024081147XtraFix® Large External Fixation System00-5210-019-0100-5210-019-012016-09-28
00889024081154XtraFix® Large External Fixation System00-5210-029-0100-5210-029-012016-09-28
00889024081178XtraFix® Large External Fixation System00-5210-040-0000-5210-040-002016-09-28
00889024081185XtraFix® Large External Fixation System00-5210-040-0100-5210-040-012016-09-28
00889024081192XtraFix® Large External Fixation System00-5210-040-0200-5210-040-022016-09-28
00889024081208XtraFix® Large External Fixation System00-5210-040-0300-5210-040-032016-09-28
00889024081215XtraFix® Large External Fixation System00-5210-040-0400-5210-040-042016-09-28
00889024081239XtraFix® Large External Fixation System00-5210-040-0600-5210-040-062016-09-28
00889024081253XtraFix® Large External Fixation System00-5210-050-0100-5210-050-012016-09-28
00889024081260XtraFix® Large External Fixation System00-5210-050-0200-5210-050-022016-09-28
00889024081277XtraFix® Large External Fixation System00-5210-050-0300-5210-050-032016-09-28
00889024081284XtraFix® Large External Fixation System00-5210-050-0400-5210-050-042016-09-28
00889024081307XtraFix® Large External Fixation System00-5210-050-0600-5210-050-062016-09-28

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
03760177046542CLEARCUTTEKNIMEDLZN2020-11-25
03760177046573CLEARCUTTEKNIMEDLZN2020-11-25
03760177046603CLEARCUTTEKNIMEDLZN2020-11-25
03760177046634CLEARCUTTEKNIMEDLZN2020-11-25
03760177046665CLEARCUTTEKNIMEDLZN2020-11-25
03760177046696CLEARCUTTEKNIMEDLZN2020-11-25
03760177046535CLEARCUTTEKNIMEDLZN2020-09-24
00889024510326NAZimmer, Inc.LZN2018-09-14
00889024510333NAZimmer, Inc.LZN2018-09-14
00889024510340NAZimmer, Inc.LZN2018-09-14
00889024510357NAZimmer, Inc.LZN2018-09-14
00889024510364NAZimmer, Inc.LZN2018-09-14
00889024510371NAZimmer, Inc.LZN2018-09-14
00888912023443DJO SURGICALEncore Medical, L.P.LZN2017-05-04
00888912023450DJO SURGICALEncore Medical, L.P.LZN2017-05-04
00888912023467DJO SURGICALEncore Medical, L.P.LZN2017-05-04
00888912023474DJO SURGICALEncore Medical, L.P.LZN2017-05-04
00888912023481DJO SURGICALEncore Medical, L.P.LZN2017-05-04
00888912073806DJO SURGICALEncore Medical, L.P.LZN2017-05-04
00889024376724NAZimmer, Inc.LZN2016-08-31
00889024376748NAZimmer, Inc.LZN2016-08-31
00889024376755NAZimmer, Inc.LZN2016-08-31
00889024432918NAZimmer, Inc.LZN2016-07-15
00889024432970NAZimmer, Inc.LZN2016-05-24
00889024432987NAZimmer, Inc.LZN2016-05-24
00889024432994NAZimmer, Inc.LZN2016-05-24
00889024433007NAZimmer, Inc.LZN2016-05-24
00889024433014NAZimmer, Inc.LZN2016-05-24
00889024433021NAZimmer, Inc.LZN2016-05-24
00889024432901N/AZimmer, Inc.LZN2016-02-04