Cayenne Medical, Inc. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Cayenne Medical, Inc. has 22 FDA 510(k) cleared orthopedic devices. Based in San Diego, US.
Historical record: 22 cleared submissions from 2006 to 2018.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
22 devices
Cleared
Mar 21, 2018
Ventix Link Knotless Anchor with Inserter
Orthopedic
49d
Cleared
Oct 16, 2017
BioWick X Implant with Driver
Orthopedic
88d
Cleared
Aug 03, 2016
AFX™ Femoral Implant With Inserter
Orthopedic
112d
Cleared
Jul 24, 2015
SureLock W Suture Anchor
Orthopedic
94d
Cleared
Mar 25, 2015
Short SureLock All-Suture Anchor, 1.4mm with (1) size 0 UHMWPE suture with...
Orthopedic
110d
Cleared
Jan 23, 2015
Quattro Bolt Tenodesis Screw
Orthopedic
58d
Cleared
Dec 30, 2013
SURELOCK ALL-SUTURE ANCHOR WITH INSERTER, 1.4MM, SURELOCK ALL-SUTURE ANCHOR...
Orthopedic
108d
Cleared
Aug 16, 2013
QUATTRO GL SUTURE ANCHOR
Orthopedic
100d
Cleared
Oct 31, 2012
QUATRO LINK KNOTLESS ANCHOR WITH INSERTER, 2.9MM-PEEK ONLY
Orthopedic
91d
Cleared
Oct 11, 2012
APERFIX AM FEMORAL IMPLANT WITH INSERTER, 9X24 APERFIX AM FEMORAL IMPLANT...
Orthopedic
59d
Cleared
Jun 04, 2012
CROSSFIX II MEMISCAL REPAIR DEVICE
General & Plastic Surgery
24d
Cleared
Jan 17, 2012
CUFFINK
Orthopedic
112d