Medical Device Manufacturer · US , Philedelphia , PA

Implanet, S.A. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 2012

Recent clearances: SQUALE, Madison Total Knee System, JAZZ PF

Total

Cleared

Denied

Implanet, S.A. has 15 FDA 510(k) cleared orthopedic devices. Based in Philedelphia, US.

Last cleared in 2023. Active since 2012.

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

Regulatory submissions have been managed by Hogan Lovells US LLP and Mcra, LLC.

Implanet, S.A. 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 - Implanet, S.A.

15 devices

1-12 of 15

Madison Total Knee System

ISS-JAZZ Screw System and JAZZ CAP SP

JAZZ System, including JAZZ Band

JAZZ CLAW System (hooks and rods) and JAZZ CLAW connector

IMPLANET Spine System (ISS)

K143731 · NKB

Orthopedic · 106d

Implanet, S.A. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Implanet, S.A.

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