Inter-Lock 234-150-509

GUDID 04546540756732

TIBIAL INTER-LOCK GUIDE 23MM BIOSTEON SCREW

STRYKER CORPORATION

Surgical drill guide, reusable

• Primary Device ID: 04546540756732
• NIH Device Record Key: 2db26a8c-26aa-4864-8f76-45565aaa732b
• Commercial Distribution Discontinuation: 2015-10-09
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Inter-Lock
• Version Model Number: 234-150-509
• Catalog Number: 234-150-509
• Company DUNS: 187502109
• Company Name: STRYKER CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: +1(866)624-4422
• Email: xx@xx.xx

Device Dimensions

• Length: 23 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540756732 [Primary]

FDA Product Code

• NBH: ACCESSORIES,ARTHROSCOPIC

Sterilization

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

[04546540756732]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-04-06
• Device Publish Date: 2015-09-09

On-Brand Devices [Inter-Lock]

• 04546540756756: TIBIAL INTER-LOCK GUIDE 35MM BIOSTEON SCREW
• 04546540756749: TIBIAL INTER-LOCK GUIDE 28MM BIOSTEON SCREW
• 04546540756732: TIBIAL INTER-LOCK GUIDE 23MM BIOSTEON SCREW
• 04546540392305: INTER-LOCK CROSS-PIN DRILL 50MM X 2.4MM DIAMETER
• 04546540392237: INTER-LOCK CROSS PIN PLLA - 50MM
• 04546540392220: INTER-LOCK CROSS PIN PLLA PACKAGING 35MM