Acromed Corp. - FDA 510(k) Cleared Devices
Recent clearances: ISOLA SPINAL SYSTEM, TIMX LOW BACK SYSTEM TITANIUM MX ROD BASED LOW BACK SYSTEM, PEDIATRIC PRC
41
Total
22
Cleared
0
Denied
FDA 510(k) Regulatory Record - Acromed Corp. Orthopedic ✕
40 devices
Cleared
Oct 21, 1998
ISOLA SPINAL SYSTEM
Orthopedic
254d
Cleared
Jun 30, 1998
TIMX LOW BACK SYSTEM TITANIUM MX ROD BASED LOW BACK SYSTEM
Orthopedic
46d
Cleared
May 29, 1998
PEDIATRIC PRC
Orthopedic
63d
Cleared
Apr 29, 1998
ACROMED TIMX PLATE BASED LOW BACK SYSTEM
Orthopedic
21d
Cleared
Apr 14, 1998
UNIVERSITY PLATE ANTERIOR SYSTEM
Orthopedic
82d
Cleared
Mar 05, 1998
KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS
Orthopedic
76d
Cleared
Oct 01, 1997
M-2 ANTERIOR PLATE SYSTEM
Orthopedic
72d
Cleared
Jun 11, 1997
ACROMED ANTERIOR CERVICAL STABILIZATION SYSTEM
Orthopedic
86d
Cleared
Jun 11, 1997
KANEDA SR ANTERIOR SPINAL SYSTEM
Orthopedic
69d
Cleared
Jun 03, 1997
EASY ROD
Orthopedic
81d
Cleared
May 08, 1997
ACROMED PEDICLE SCREW
Orthopedic
139d
Cleared
Apr 03, 1997
ACROMED ANTERIOR CERVICAL STABILIZATION SYSTEM
Orthopedic
56d
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