Medical Device Manufacturer · US , Washington , DC

Skeletal Kinetics, LLC - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2003

Total

Cleared

Denied

Skeletal Kinetics, LLC has 10 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 10 cleared submissions from 2003 to 2017. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Skeletal Kinetics, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Skeletal Kinetics, LLC

10 devices

1-10 of 10

SKAFFOLD NMX BONE VOID FILLER

CALLOS PROMODEL BONE VOID FILLER, SKAFFOLD MP (MACRO POROUS) BONE VOID FILLER

General & Plastic Surgery · 145d

Cleared Jul 20, 2010

CALLOS BONE VOID FILLER, SKAFFOLD NEXT GENERATION BONE VOID FILLER, OSTEO VATION

K100986 · MQV

Orthopedic · 102d

Cleared Jul 20, 2005

OSTEOVATION CMF BONE VOID FILLER

K051784 · GXP

General & Plastic Surgery · 19d

Cleared Jun 03, 2005

CALLOS IMPACT AND INJECT BONE VOID FILLER

K051123 · MQV

Orthopedic · 31d

Cleared Sep 16, 2004

CALLOS CMF BONE VOID FILLER

Skeletal Kinetics, LLC - FDA 510(k) Cleared Devices

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