Figure 8 Sternotomy Closure Device

FDA 510(k) K110541 · Figure 8 Surgical, Incorporated

Substantially Equivalent

510(k) numberK110541

Submission

Device name
Figure 8 Sternotomy Closure Device
Applicant
Figure 8 Surgical, Incorporated
Sunnyvale, CA, US
Received
February 25, 2011
Decision date
July 6, 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
JDQ – Cerclage, Fixation
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3010
Specialty
Orthopedic
Implant
Yes

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K232986VariTrax Sternal CircumFixation SystemJDQ · Traditional Circumfix Solutions, Inc.01/30/2024SE
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K231333STRETTO™ Cable SystemJDQ · Traditional Globus Medical, Inc.08/04/2023SE
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Questions and answers

When was Figure 8 Sternotomy Closure Device cleared by the FDA?

Figure 8 Sternotomy Closure Device (K110541) received a 510(k) decision of Substantially Equivalent on July 6, 2011, 131 days after the submission was received.

What is the product code of K110541?

The FDA product code is JDQ – Cerclage, Fixation, a Class II (moderate risk) device regulated under 21 CFR 888.3010.