Medical Device Manufacturer · US , Sturgeon Bay , WI

Parcus Medical, LLC - FDA 510(k) Cleared Devices

28 submissions · 28 cleared · Since 2009

Recent clearances: Parcus Synd-EZ SS, X-Twist PEEK Suture Anchor, ActiFlip

Total

Cleared

Denied

Parcus Medical, LLC has 28 FDA 510(k) cleared orthopedic devices. Based in Sturgeon Bay, US.

Last cleared in 2022. Active since 2009.

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

Parcus Medical, 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 - Parcus Medical, LLC

28 devices

1-12 of 28

X-Twist PEEK Suture Anchor

Parcus Titanium Interference Screws

K202662 · MBI

Orthopedic · 161d

Cleared Oct 28, 2020

Parcus GFS II and GFS Mini, GFS Naked, GFS Ultimate, GFS BTB, ATLAS, Synd-EZ...

K202259 · MBI

Orthopedic · 79d

Cleared Jul 23, 2020

Parcus V-lox Titanium Suture Anchors, Parcus Miti Suture Anchors

K201083 · MBI

Orthopedic · 91d

Cleared Jan 23, 2020

Parcus Knotless PEEK and PEEK CF Push-In Suture Anchor

K193295 · MBI

Orthopedic · 57d

Cleared Jan 16, 2020

AcTiFlip Naked, AcTiFlip Cinch, AcTiFlip WHIP, GFS Ultimate Hip

Parcus Knotless AP Suture Anchors

Parcus Medical, LLC - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Parcus Medical, LLC

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