Cormet 2000 Hemi-Hip Metallic Resurfacing Prosthes S279.860

GUDID 05055196932425

MODULAR INTRODUCER BASE PLATE SIZE 9/60-62mm

CORIN LTD

Orthopaedic implant/instrument adaptor, reusable

• Primary Device ID: 05055196932425
• NIH Device Record Key: b7f913bb-6d3e-49fe-876f-9f592d24dcc6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cormet 2000 Hemi-Hip Metallic Resurfacing Prosthes
• Version Model Number: S279.860
• Catalog Number: S279.860
• Company DUNS: 295437313
• Company Name: CORIN LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +441285659866
• Email: rachel.king@coringroup.com
• Phone: +441285659866
• Email: rachel.king@coringroup.com
• Phone: +441285659866
• Email: rachel.king@coringroup.com
• Phone: +441285659866
• Email: rachel.king@coringroup.com
• Phone: +441285659866
• Email: rachel.king@coringroup.com
• Phone: +441285659866
• Email: rachel.king@coringroup.com
• Phone: +441285659866
• Email: rachel.king@coringroup.com
• Phone: +441285659866
• Email: rachel.king@coringroup.com
• Phone: +441285659866
• Email: rachel.king@coringroup.com
• Phone: +441285659866
• Email: rachel.king@coringroup.com
• Phone: +441285659866
• Email: rachel.king@coringroup.com
• Phone: +441285659866
• Email: rachel.king@coringroup.com
• Phone: +441285659866
• Email: rachel.king@coringroup.com
• Phone: +441285659866
• Email: rachel.king@coringroup.com
• Phone: +441285659866
• Email: rachel.king@coringroup.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05055196932425 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K994153

FDA Product Code

• KXA: Prosthesis, hip, femoral, resurfacing

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[05055196932425]

Moist Heat or Steam Sterilization

[05055196932425]

Moist Heat or Steam Sterilization

[05055196932425]

Moist Heat or Steam Sterilization

[05055196932425]

Moist Heat or Steam Sterilization

[05055196932425]

Moist Heat or Steam Sterilization

[05055196932425]

Moist Heat or Steam Sterilization

[05055196932425]

Moist Heat or Steam Sterilization

[05055196932425]

Moist Heat or Steam Sterilization

[05055196932425]

Moist Heat or Steam Sterilization

[05055196932425]

Moist Heat or Steam Sterilization

[05055196932425]

Moist Heat or Steam Sterilization

[05055196932425]

Moist Heat or Steam Sterilization

[05055196932425]

Moist Heat or Steam Sterilization

[05055196932425]

Moist Heat or Steam Sterilization

[05055196932425]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-08-17

On-Brand Devices [Cormet 2000 Hemi-Hip Metallic Resurfacing Prosthes]

• 05055343887622: ACETABULAR REAMER 60MM
• 05055343887578: ACETABULAR REAMER DRIVE SHAFT
• 05055343887561: ACETABULAR REAMER 54MM
• 05055343887554: ACETABULAR REAMER 53MM
• 05055343887547: ACETABULAR REAMER 52MM
• 05055343887530: ACETABULAR REAMER 51MM
• 05055343887523: ACETABULAR REAMER 50MM
• 05055343887516: ACETABULAR REAMER 49MM
• 05055343887509: ACETABULAR REAMER 48MM
• 05055343887493: ACETABULAR REAMER 47MM
• 05055343887486: ACETABULAR REAMER 46MM
• 05055343887479: ACETABULAR REAMER 45MM
• 05055343887462: ACETABULAR REAMER 44MM
• 05055343887455: ACETABULAR REAMER 43MM
• 05055343887448: ACETABULAR REAMER 42MM
• 05055343887431: ACETABULAR REAMER 41MM
• 05055343887424: ACETABULAR REAMER 40MM
• 05055343887417: ACETABULAR REAMER 39MM
• 05055343887400: ACETABULAR REAMER 38MM
• 05055343887332: ACETABULAR REAMER 64MM
• 05055343887325: ACETABULAR REAMER 63MM
• 05055343887318: ACETABULAR REAMER 62MM
• 05055343887301: ACETABULAR REAMER 61MM
• 05055343887295: ACETABULAR REAMER 59MM
• 05055343887288: ACETABULAR REAMER 58MM
• 05055343887271: ACETABULAR REAMER 57MM
• 05055343887264: ACETABULAR REAMER 56MM
• 05055343887257: ACETABULAR REAMER 55MM
• 05055343878422: CANNULATED DRILL STRYKER DRIVE
• 05055343878415: MODULAR DRIVE SHAFT STRYKER DRIVE
• 05055343832110: ACETABULAR SIZER SIZE 64MM
• 05055196942615: ACETABULAR SIZER SIZE 50MM
• 05055196942608: ACETABULAR SIZER SIZE 48MM
• 05055196942592: ACETABULAR SIZER SIZE 46MM
• 05055196942585: ACETABULAR SIZER SIZE 60MM
• 05055196942578: ACETABULAR SIZER SIZE 58MM
• 05055196942561: ACETABULAR SIZER SIZE 56MM
• 05055196942554: ACETABULAR SIZER SIZE 54MM
• 05055196942547: ACETABULAR SIZER SIZE 52MM
• 05055196942530: ACETABULAR SIZER SIZE 62MM
• 05055196941809: SI HEAD ALIGNMENT STYLUS SIZES 3, 5, 7 & 9
• 05055196941793: SI HEAD ALIGNMENT STYLUS SIZES 2, 4, 6, 8 & 10
• 05055196940444: INTRODUCER ALIGNMENT ROD
• 05055196940390: INTRODUCER TOMMY BAR
• 05055196939820: HEAD FINISHING REAMER - STRYKER DRIVE
• 05055196939806: HEAD FINISHING REAMER A/O DRIVE
• 05055196932425: MODULAR INTRODUCER BASE PLATE SIZE 9/60-62mm
• 05055196932418: MODULAR INTRODUCER BASE PLATE SIZE 7/56-58mm
• 05055196932401: MODULAR INTRODUCER BASE PLATE SIZE 5/52-54mm
• 05055196932395: MODULAR INTRODUCER BASE PLATE SIZE 3/48-50mm