AVS 48389100

GUDID 07613327270280

TL SPACER INSERTER STRAIGHT

Stryker Corporation

Orthopaedic inorganic implant inserter/extractor, reusable

• Primary Device ID: 07613327270280
• NIH Device Record Key: 30413f74-6ce9-457e-b55c-cd45a6f855ac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AVS
• Version Model Number: 48389100
• Catalog Number: 48389100
• Company DUNS: 149183167
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327270280 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[07613327270280]

Moist Heat or Steam Sterilization

[07613327270280]

Moist Heat or Steam Sterilization

[07613327270280]

Moist Heat or Steam Sterilization

[07613327270280]

Moist Heat or Steam Sterilization

[07613327270280]

Moist Heat or Steam Sterilization

[07613327270280]

Moist Heat or Steam Sterilization

[07613327270280]

Moist Heat or Steam Sterilization

[07613327270280]

Moist Heat or Steam Sterilization

[07613327270280]

Moist Heat or Steam Sterilization

[07613327270280]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-09-11
• Device Publish Date: 2019-11-22

On-Brand Devices [AVS]

• 07613327267945: PL GRAFT BLOCK
• 07613327267693: AL SPACER SUPPORT
• 07613327267624: AS SPACER SUPPORT
• 07613327122169: PL TRIAL INSTRUMENT INSERT
• 07613327121193: TL PEEK CONTAINER
• 07613327120950: WIDE IMPLANT TRAY
• 07613327120943: IMPLANT TRAY
• 07613327119572: LID LONG IMPLANT SIZES
• 07613327119558: WIDE IMPLANT TRAY
• 07613327119541: WIDE IMPLANT TRAY
• 07613327119527: PL PEEK IMPLANT CONTAINER
• 07613327119503: PL PEEK INSTRUMENT CONTAINER
• 07613327119480: INSTRUMENTBASE
• 07613327119473: PL PEEK CONTAINER
• 07613327119466: PL PEEK CONTAINER
• 07613327119428: AL PEEK CONTAINER
• 07613327119411: AS PEEK CONTAINER
• 07613327270556: SPACER TRIAL
• 07613327270518: SPACER TRIAL
• 07613327270471: SPACER TRIAL
• 07613327270457: SPACER TRIAL
• 07613327270440: SPACER TRIAL
• 07613327270433: SPACER TRIAL
• 07613327270426: SPACER TRIAL
• 07613327270419: SPACER TRIAL
• 07613327270402: SPACER TRIAL
• 07613327270372: SPACER TRIAL
• 07613327270358: SPACER TRIAL
• 07613327270334: SPACER TRIAL
• 07613327268546: UniLIF TRIAL
• 07613327268270: UniLIF TRIAL
• 07613327268263: UniLIF TRIAL
• 07613327268256: UniLIF TRIAL
• 07613327268249: UniLIF TRIAL
• 07613327268232: UniLIF TRIAL
• 07613327268225: UniLIF TRIAL
• 07613327268218: UniLIF TRIAL
• 07613327268201: UniLIF TRIAL
• 07613327268195: UniLIF TRIAL
• 07613327268188: UniLIF TRIAL
• 07613327268171: UniLIF TRIAL
• 07613327268164: UniLIF TRIAL
• 07613327268157: UniLIF TRIAL
• 07613327268140: UniLIF TRIAL
• 07613327268133: UniLIF TRIAL
• 07613327268126: UniLIF TRIAL
• 07613327268119: UniLIF TRIAL
• 07613327268102: UniLIF TRIAL
• 07613327268096: UniLIF TRIAL
• 07613327268089: UniLIF TRIAL