Spinefrontier, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spinefrontier, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SpineFrontier Lumbar Interbody Fusion Device System, A-CIFT SoloFuse
24
Total
24
Cleared
0
Denied
Spinefrontier, Inc. has 24 FDA 510(k) cleared orthopedic devices. Based in Beverly, US.
Historical record: 24 cleared submissions from 2007 to 2020.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Testing Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Spinefrontier, Inc.
24 devices
Cleared
Jun 19, 2020
SpineFrontier Lumbar Interbody Fusion Device System
Orthopedic
224d
Cleared
May 08, 2018
A-CIFT SoloFuse
Orthopedic
264d
Cleared
Jul 17, 2015
A-CIFT SoloFuse
Orthopedic
73d
Cleared
May 13, 2015
SpineFrontier Lumbar Interbody Fusion Device System
Orthopedic
250d
Cleared
Apr 24, 2015
SpineFrontier SIJFuse Sacroiliac Joint Fusion Device System
Orthopedic
109d
Cleared
Feb 12, 2015
PedFuse Pedicle Screw System
Orthopedic
79d
Cleared
Nov 25, 2014
ARENA-C TIFUSE CERVICAL INTERVERTEBRAL BODY FUSION DEVICE
Orthopedic
188d
Cleared
Oct 20, 2014
SPINEFRONTIER ARENA-C HA PEEK CERVICAL INTERVERTEBRAL BODY FUSION DEVICE
Orthopedic
87d
Cleared
Sep 08, 2014
ARENA-C
Orthopedic
110d
Cleared
May 14, 2014
SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEM
Orthopedic
209d
Cleared
Jan 03, 2014
SPINEFRONTIER A-CIFT SOLOFUSE CERVICAL INTERVERTEBRAL FUSION DEVICE SYSTEM
Orthopedic
192d
Cleared
Nov 26, 2013
SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEM
Orthopedic
84d