Parcus 2.0MM / 2.5MM / 3.5MM Miti Titanium Suture Anchor

FDA 510(k) K111000 · Parcus Medical, LLC

Substantially Equivalent

510(k) numberK111000

Submission

Device name
Parcus 2.0MM / 2.5MM / 3.5MM Miti Titanium Suture Anchor
Applicant
Parcus Medical, LLC
Sturgeon Bay, WI, US
Received
April 11, 2011
Decision date
July 28, 2011
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HWC – Screw, Fixation, Bone
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3040
Specialty
Orthopedic
Implant
Yes

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More from Arthrex, Inc.

510(k)DeviceDecision
K232513X-Twist Biocomposite Suture AnchorMAI · Special 09/18/2023SE
K221502Parcus Synd-EZ SSMBI · Traditional 07/26/2022SE
K221135X-Twist PEEK Suture AnchorMBI · Special 05/19/2022SE
K212739ActiFlipMBI · Traditional 10/06/2021SE
K202662Parcus Titanium Interference ScrewsMBI · Traditional 02/22/2021SE
K202259Parcus GFS II and GFS Mini, GFS Naked, GFS Ultimate, GFS BTB, ATLAS, Synd-EZ Ti…MBI · Traditional 10/28/2020SE
K201083Parcus V-lox Titanium Suture Anchors, Parcus Miti Suture AnchorsMBI · Traditional 07/23/2020SE
K193295Parcus Knotless PEEK and PEEK CF Push-In Suture AnchorMBI · Special 01/23/2020SE
K192750AcTiFlip Naked, AcTiFlip Cinch, AcTiFlip WHIP, GFS Ultimate HipMBI · Traditional 01/16/2020SE
K192964Parcus Synd-EZ SSMBI · Special 11/22/2019SE

Questions and answers

When was Parcus 2.0MM / 2.5MM / 3.5MM Miti Titanium Suture Anchor cleared by the FDA?

Parcus 2.0MM / 2.5MM / 3.5MM Miti Titanium Suture Anchor (K111000) received a 510(k) decision of Substantially Equivalent on July 28, 2011, 108 days after the submission was received.

What is the product code of K111000?

The FDA product code is HWC – Screw, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3040.