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.

Skeletal Kinetics, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

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

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