Medical Device Manufacturer · US , Miami , FL

Hand Innovations, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2000
10
Total
10
Cleared
0
Denied

Hand Innovations, Inc. has 10 FDA 510(k) cleared orthopedic devices. Based in Miami, US.

Historical record: 10 cleared submissions from 2000 to 2005.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Hand Innovations, Inc.
10 devices
1-10 of 10
Cleared Apr 26, 2005
DISTAL VOLAR RADIUS ANATOMICAL PLATE SYSTEM
K050932 · LXT
Orthopedic · 12d
Cleared Sep 30, 2004
SHOULDER FIXATION SYSTEM
K042059 · LXT
Orthopedic · 62d
Cleared Jul 30, 2004
MODIFICATION TO SMALL BONE FIXATION SYSTEM
K041157 · HTY
Orthopedic · 88d
Cleared Jul 01, 2004
FRAGMENT PLATE SYSTEM, SCREWS, PINS AND K-WIRES
K041081 · KTT
Orthopedic · 66d
Cleared Jan 15, 2004
SMALL BONE FIXATION SYSTEM
K033406 · HTY
Orthopedic · 83d
Cleared Oct 01, 2003
DISTAL RADIUS FRACTURE REPAIR SYSTEM
K032705 · LXT
Orthopedic · 29d
Cleared Apr 01, 2003
HAND INNOVATIONS, INC. DISTAL RADIUS FRACTURE REPAIR SYSTEM
K030198 · HRS
Orthopedic · 70d
Cleared Dec 05, 2002
DISTAL RADIUS FRACTURE REPAIR SYSTEM
K023007 · HRS
Orthopedic · 87d
Cleared Dec 20, 2001
INTRAMEDULLARY FIXATION SYSTEM FOR THE HAND
K013424 · HTY
Orthopedic · 66d
Cleared Dec 05, 2000
DISTAL VOLAR RADIUS FRACTURE REPAIR SYSTEM
K002775 · HRS
Orthopedic · 90d
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