Medical Device Manufacturer · US , Minneapolis , MN

Zimmer Spine, Inc. - FDA 510(k) Cleared Devices

38 submissions · 35 cleared · Since 2004
38
Total
35
Cleared
0
Denied

Zimmer Spine, Inc. has 35 FDA 510(k) cleared orthopedic devices. Based in Minneapolis, US.

Historical record: 35 cleared submissions from 2004 to 2016.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Zimmer Spine, Inc.
38 devices
1-12 of 38
Cleared Feb 16, 2016
Zimmer Virage OCT Spinal Fixation System
K153631 · NKG
Orthopedic · 60d
Cleared Aug 31, 2015
Vitality Spinal Fixation System
K150896 · NKB
Orthopedic · 151d
Cleared Jun 24, 2015
Virage OCT Spinal Fixation System
K151031 · NKG
Orthopedic · 68d
Cleared Jun 18, 2015
Minit Posterior Cervical-Thoracic Fixation System, Nex-Link Spinal Fixation...
K142752 · NKB
Orthopedic · 267d
Cleared Mar 20, 2015
inVizia Anterior Certical Plate System, SC-AcuFix Ant-Cer Dynamic Cervical...
K143626 · KWQ
Orthopedic · 88d
Cleared Feb 12, 2015
Ardis Interbody System, BAK Interbody Fusion System, BAK/C Anterior Cervical...
K143297 · MAX
Orthopedic · 87d
Cleared Oct 29, 2014
UNIVERSAL CLAMP SPINAL FIXATION SYSTEM
K142053 · OWI
Orthopedic · 92d
Cleared Sep 23, 2014
OPTIO-C ANTERIOR CERVICAL SYSTEM
K141500 · KWQ
Orthopedic · 109d
Cleared Jun 02, 2014
VIRAGE OCT SPINAL FIXATION SYSTEM
K133556 · KWP
Orthopedic · 195d
Cleared May 21, 2014
TRINICA ANTERIOR LUMBAR PLATE SYSTEM
K140611 · KWQ
Orthopedic · 72d
Cleared Jan 30, 2014
ARDIS INTERBODY SYSTEM
K133184 · MAX
Orthopedic · 105d
Cleared Jan 16, 2014
OPTIO-C ANTERIOR CERVICAL SYSTEM
K132894 · OVE
Orthopedic · 122d

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