ClearanceBrief
Company ยท DE

Biedermann Motech GmbH & Co. KG

FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 2021. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
NKBThoracolumbosacral Pedicle Screw System3
EZXMesh, Surgical, Metal1
JDNImplant, Fixation Device, Spinal1
MAXIntervertebral Fusion Device With Bone Graft, Lumbar1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 20, 2021K203607MOSS VRS Spinal System
Biedermann Motech GmbH & Co. KG, DE
NKB
Sep 13, 2018K181821MOSS VRS Spinal System
Biedermann Motech GmbH & Co. KG, DE
NKB
Jun 2, 2017K170890TELIX K Interbody System
Biedermann Motech GmbH & Co. KG, DE
MAX
Nov 17, 2016K162232MOSS 100 Pedicle Screw System
Biedermann Motech GmbH & Co. KG, DE
NKB
Apr 25, 1990K894184BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEM
Biedermann Motech GmbH, DE
JDN
Mar 20, 1990K900138MOTECH TITANIUM SURGICAL MESH
Biedermann Motech GmbH
EZX

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes