Rotation Medical, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Rotation Medical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 5 cleared submissions from 2011 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Rotation Medical, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Mar 26, 2014
COLLAGEN TENDON SHEET-DDI (CTS-DDI)
Orthopedic
48d
Cleared
Aug 29, 2013
ROTATION MEDICAL BONE STAPLE (RMB STAPLE)
Orthopedic
86d
Cleared
Jul 12, 2013
ROTATION MEDICAL SOFT TISSUE STAPLE (RMST STAPLE)
General & Plastic Surgery
38d
Cleared
Jan 08, 2013
COLLAGEN TENDON SHEET-D
General & Plastic Surgery
180d
Cleared
Dec 22, 2011
COLLAGEN TENDON SHEET
General & Plastic Surgery
121d