MCGEE PISTON SHEPHERD'S CROOK STYLE 4 MM LENGTH SLIM 6 MM DIA STAINLESS

GUDID 00821925017641

Gyrus Acmi, Inc.

Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material

• Primary Device ID: 00821925017641
• NIH Device Record Key: 6874cc95-365c-4138-8aa9-44c4865bf2eb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MCGEE PISTON SHEPHERD'S CROOK STYLE 4 MM LENGTH SLIM 6 MM DIA STAINLESS
• Version Model Number: 140475
• Company DUNS: 007198742
• Company Name: Gyrus Acmi, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx
• Phone: 1(800)262-3540
• Email: xxx@xxx.xxx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00821925017641 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K760433

FDA Product Code

• ETA: Replacement, Ossicular Prosthesis, Total

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-24