Medical Device Manufacturer · US , Stillwater , MN

Spineology, Inc. - FDA 510(k) Cleared Devices

54 submissions · 51 cleared · Since 1999
54
Total
51
Cleared
1
Denied
53 devices
51-53 of 53
Cleared Jul 06, 2004
OPTIMESH 500E CEMENT RESTRICTOR
K033953 · JDK
Orthopedic · 197d
Cleared Sep 15, 2000
K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM
K002371 · KWQ
Orthopedic · 50d
Cleared Dec 27, 1999
K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM
K990959 · KWQ
Orthopedic · 280d
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