Px®

GUDID M711LS2630

SST

Innovasis, Inc.

Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable

• Primary Device ID: M711LS2630
• NIH Device Record Key: b94fa6d0-9ab1-49fa-b6a4-3fede7883ee7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Px®
• Version Model Number: LS-263
• Company DUNS: 156567492
• Company Name: Innovasis, Inc.
• 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: false
• Serial Number: true
• 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: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com
• Phone: 801-261-2236
• Email: info@innovasis.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M711LS2630 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150500

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

[M711LS2630]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-04-08
• Device Publish Date: 2022-03-31

On-Brand Devices [Px®]

• M711LS1810: Al, Silicone, SST
• M711LS2630: SST
• M711BTA1180: Crosslink Polyethylene, Convoluted Polyurethene, Lexan
• M711LS26590: SST
• M711LS26580: SST
• M711LS265160: SST
• M711LS265150: SST
• M711LS265140: SST
• M711LS265130: SST
• M711LS265120: SST
• M711LS265110: SST
• M711LS265100: SST
• M711LS26490: SST
• M711LS26480: SST
• M711LS264160: SST
• M711LS264150: SST
• M711LS264140: SST
• M711LS264130: SST
• M711LS264120: SST
• M711LS264110: SST
• M711LS264100: SST
• M711LS26190: SST
• M711LS26180: SST
• M711LS261160: SST
• M711LS261150: SST
• M711LS261140: SST
• M711LS261130: SST
• M711LS261120: SST
• M711LS261110: SST
• M711LS261100: SST
• M711LS2580: Silicone, SST
• M711LS2110: Silicone, SST
• M711LS2160: SST
• M711LS2150: Tecapro mt.
• M711LS21090: SST
• M711LS21080: SST
• M711LS21070: SST
• M711LS210160: SST
• M711LS210150: SST
• M711LS210140: SST
• M711LS210130: SST
• M711LS210120: SST
• M711LS210110: SST
• M711LS210100: SST
• M711LS20990: SST
• M711LS20980: SST
• M711LS209160: SST
• M711LS209150: SST
• M711LS209140: SST
• M711LS209130: SST