MC+ MC907R

GUDID 03662663043588

LDR Spine Usa, Inc.

Tendon/ligament graft preparation station

• Primary Device ID: 03662663043588
• NIH Device Record Key: 933df893-1d16-4e7f-88fe-c7d77a61cb45
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MC+
• Version Model Number: MC907R
• Catalog Number: MC907R
• Company DUNS: 615789729
• Company Name: LDR Spine Usa, 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: 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: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	03662663043588 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121103

FDA Product Code

• NKB: Thoracolumbosacral Pedicle Screw System

Sterilization

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

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

[03662663043588]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2022-03-10
• Device Publish Date: 2018-12-12

On-Brand Devices [MC+]

• 03662663022132: MC+ CLOSED V.B.R. 12x15.5H7MM
• 03662663022125: MC+ CLOSED V.B.R. 12x15.5H6MM
• 03662663022118: MC+ CLOSED V.B.R. 12x15. 5H5 MM
• 03662663022101: MC+ CLOSED V.B.R. 12x15. 5H4,5 MM
• 03662663022064: MC+ CLOSED V.B.R.12X14 H7 MM
• 03662663022057: MC+ CLOSED V.B.R.12X14 H6 MM
• 03662663022040: MC+ CLOSED V.B.R. 12X14 H5 MM
• 03662663022033: MC+ CLOSED V.B.R. 12X14 H4.5 MM
• 03662663021999: MC+ CLOSED V.B.R.14x17 H7 MM
• 03662663021982: MC+ CLOSED V.B.R. 14x17 H6 MM
• 03662663021975: MC+ CLOSED V.B.R. 14x17 H5 MM
• 03662663021937: MC+ CLOSED V.B.R.14x15.5 H7 MM
• 03662663021920: MC+ CLOSED V.B.R.14x15.5 H6 MM
• 03662663021913: MC+ CLOSED V.B.R.14x15.5 H5 MM
• 03662663021906: MC+ CLOSED V.B.R.14x15.5 H4.5 MM
• 03662663021869: MC+ CLOSED V.B.R. 14x14 H7 MM
• 03662663021852: MC+ CLOSED V.B.R.14x14 H6 MM
• 03662663021845: MC+ CLOSED V.B.R.14x14 H5 MM
• 03662663021838: MC+ CLOSED V.B.R.14X14 H4.5 MM
• 03662663021821: MC+ OPEN V.B.R.12X15.5H7MM
• 03662663021814: MC+ OPEN V.B.R.12X15.5H6MM
• 03662663021807: MC+ OPEN V.B.R.12X15.5H5MM
• 03662663021760: MC+ OPEN V.B.R.14x17 H7 MM
• 03662663021753: MC+ OPEN V.B.R.14x17 H6 MM
• 03662663021746: MC+ OPEN V.B.R.14x17 H5 MM
• 03662663021739: MC+ OPEN V.B.R.14x15.5 H7MM
• 03662663021722: MC+ OPEN V.B.R.14x15.5 H6 MM
• 03662663021708: MC+ OPEN V.B.R.14X14 H7 MM
• 03662663021692: MC+ OPEN V.B.R.14X14 H6 MM
• 03662663021685: MC+ OPEN V.B.R.14X14 H5 MM
• 03662663044158: MC936R
• 03662663043687: MC909R
• 03662663043304: MC901R
• 03662663046077: MC990
• 03662663045506: MC928R
• 03662663045490: MC906R
• 03662663044332: MC960R
• 03662663044325: TRIAL CERVICAL IMPLANT 12X15.5 H10 MM
• 03662663044318: TRIAL CERVICAL IMPLANT 12X15.5 H9 MM
• 03662663044301: TRIAL CERVICAL IMPLANT 12X15.5 H8 MM
• 03662663044295: TRIAL CERVICAL IMPLANT 12X14 H10 MM
• 03662663044288: TRIAL CERVICAL IMPLANT 12X14 H9 MM
• 03662663044271: TRIAL CERVICAL IMPLANT 12X14 H8 MM
• 03662663044264: TRIAL CERVICAL IMPLANT 14X17 H10 MM
• 03662663044257: TRIAL CERVICAL IMPLANT 14X17 H9 MM
• 03662663044240: TRIAL CERVICAL IMPLANT 14X17 H8 MM
• 03662663044233: TRIAL CERVICAL IMPLANT 14X15.5 H10 MM
• 03662663044226: TRIAL CERVICAL IMPLANT 14X15.5 H9 MM
• 03662663044219: TRIAL CERVICAL IMPLANT 14X15.5 H8 MM
• 03662663044202: TRIAL CERVICAL IMPLANT 14X14 H10 MM