FDA.reportPublic FDA data

TM ANK LAT CUT GDE FRAME SLIDE LOCK BOLT

Primary DI
00889024646292
Brand
TM ANK LAT CUT GDE FRAME SLIDE LOCK BOLT
Company
Zimmer, Inc.
Model
SSI006792
Catalog number
SSI006792
Published
2022-06-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HSNProsthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HSNProsthesis, Ankle, Semi-Constrained, Cemented, Metal/PolymerOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K120906000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K120906000ZIMMER TRABECULAR METAL TOTAL ANKLEZimmer, Inc.2012-08-24HSN

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00889024646292PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00889024646292008890246462928890246462920889024646292

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic prosthesis implantation instrument, reusableA hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments. It may be used for the following applications: 1) to hold/align/fix bone preparation instruments, prosthesis, or prosthesis component; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface between prosthesis components. This is a reusable device intended to be sterilized prior to use.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
1 (800) 343-9500customerservice@zimmerbiomet.com

Regulatory Flags#

DUNS number
056038268
Device count
1
Serial number
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00889024707382Persona Tensor Sizer Arm – LongSSI008513SSI0085132026-05-29
00889024707399Persona Tensor Sizer Arm – StdSSI008567SSI0085672026-05-29
00889024707405Persona Tensor Sizer BodySSI008566SSI0085662026-05-29
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

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
10381780237730Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237747Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237754Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237761Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237778Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237785Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237792Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237808Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237815Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237822Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237839Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237846Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237853Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237860Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237877Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237884Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237891Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237907Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237914Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237921Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237938Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237945Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237952Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237969Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237976Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237983Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780237990Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780238003Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780238010Cadence™Ascension Orthopedics, Inc.HSN2016-01-12
10381780238027Cadence™Ascension Orthopedics, Inc.HSN2016-01-12