Zimmer Biomet Spine Inc 10225 Westmoor Drivewestminster Co 80021 Pma Numberp110009 Supplement Numbers032 Date Received01 21 2022 Decision Date11 09 2022 Product Code Mjo Advisory Committee Orthopedic Supplement Type135 Review Track For 30 Day Notice Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No

FDA Filings

This page includes the latest FDA filings for Zimmer Biomet Spine Inc 10225 Westmoor Drivewestminster Co 80021 Pma Numberp110009 Supplement Numbers032 Date Received01 21 2022 Decision Date11 09 2022 Product Code Mjo Advisory Committee Orthopedic Supplement Type135 Review Track For 30 Day Notice Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Filings

Device Company	Device	Date
PMA P110009S032 Zimmer Biomet Spine, Inc.10225 Westmoor Drivewestminster, CO 80021 PMA NumberP110009 Supplement NumberS032 Date Received01/21/2022 Decision Date11/09/2022 Product Code MJO  Advisory Committee Orthopedic Supplement Type135 Review Track For 30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	LDR Spine Mobi-C® Cervical Disc Prosthesis	2022-11-09