Renovo Life Small Bone IM Nail System

FDA 510(k) K161254 · Renovo Life, LLC

Substantially Equivalent

510(k) numberK161254

Submission

Device name
Renovo Life Small Bone IM Nail System
Applicant
Renovo Life, LLC
Belmont, NC, US
Received
May 3, 2016
Decision date
November 7, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HSB – Rod, Fixation, Intramedullary And Accessories
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3020
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was Renovo Life Small Bone IM Nail System cleared by the FDA?

Renovo Life Small Bone IM Nail System (K161254) received a 510(k) decision of Substantially Equivalent on November 7, 2016, 188 days after the submission was received.

What is the product code of K161254?

The FDA product code is HSB – Rod, Fixation, Intramedullary And Accessories, a Class II (moderate risk) device regulated under 21 CFR 888.3020.