Signus Medizintechnik is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Signus Medizintechnik - FDA 510(k) Cleared Devices
Recent clearances: VERTACONNECT TLIF Cage
1
Total
1
Cleared
0
Denied
Signus Medizintechnik has 1 FDA 510(k) cleared medical devices. Based in Alzenau, DE.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Signus Medizintechnik Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by The OrthoMedix Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Signus Medizintechnik
1 devices