Medical Device Manufacturer · US , San Diego , CA

Avanta Orthopaedics, Inc. - FDA 510(k) Cleared Devices

18 submissions · 17 cleared · Since 1997

Total

Cleared

Denied

Avanta Orthopaedics, Inc. has 17 FDA 510(k) cleared orthopedic devices. Based in San Diego, US.

Historical record: 17 cleared submissions from 1997 to 2003.

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 - Avanta Orthopaedics, Inc.

18 devices

1-18 of 18

Cleared Apr 10, 2003

AVANTA CARPAL FUSION PLATING SYSTEM

MODIFICATION TO RADIAL HEAD IMPLANT

K023604 · KWI

Orthopedic · 30d

Cleared Jan 25, 2002

FINGER JOINT PROSTHESIS

SCAPHIX, STAPLE, FIXATION, BONE

DISTAL RADIUS FRACTURE FIXATION PLATE SYSTEM

DISTAL RADIUS FRACTURE FIXATION PLATE

AVANTA ORTHOPAEDICS TRAPEZIUM IMPLANT

K965204 · KYI

Orthopedic · 159d

Cleared Mar 25, 1997

AVANTA ORTHOPAEDICS TENDON SPACER

K964359 · HXA

Orthopedic · 144d

Cleared Jan 22, 1997

AVANTA ORTHOPAEDICS TRAPEZIAL IMPLANT

K964381 · KYI

Orthopedic · 79d

Avanta Orthopaedics, Inc. - FDA 510(k) Cleared Devices

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