CTC Tcat(R)-Tplan(R) Surgical System

FDA 510(k) K140585 · Curexo Technology Corporation

Substantially Equivalent

510(k) numberK140585

Submission

Device name
CTC Tcat(R)-Tplan(R) Surgical System
Applicant
Curexo Technology Corporation
Melrose, MA, US
Received
March 7, 2014
Decision date
August 18, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OJP – Orthopedic Computer Controlled Surgical System
Device class
Class II (moderate risk)
Regulation
21 CFR 882.4560
Specialty
Neurology

Pre-operative planning and intra-operative execution of surgical movements with robotically controlled end effectors under user supervision. Alternative to manual planning and broaching/reaming techniques for femoral canal preparation in primary total hip arthroplasty (THA).

Other 510(k)s with product code OJP

510(k)DeviceApplicantDecision
K150741TSolution One w/ACG surgical SystemOJP · Traditional THINK Surgical, Inc.10/22/2015SE
K140038Digimatch Orthodoc Robodoc Encore Surgical SystemOJP · Traditional Curexo Technology Corporation05/27/2014SE
K072629Digimatch Robodoc Surgical SystemOJP · Traditional Integrated Surgical Systems, Inc.08/06/2008SE

More from Integrated Surgical Systems, Inc.

510(k)DeviceDecision
K140038Digimatch Orthodoc Robodoc Encore Surgical SystemOJP · Traditional 05/27/2014SE

Questions and answers

When was CTC Tcat(R)-Tplan(R) Surgical System cleared by the FDA?

CTC Tcat(R)-Tplan(R) Surgical System (K140585) received a 510(k) decision of Substantially Equivalent on August 18, 2014, 164 days after the submission was received.

What is the product code of K140585?

The FDA product code is OJP – Orthopedic Computer Controlled Surgical System, a Class II (moderate risk) device regulated under 21 CFR 882.4560.