Cfn-Cannulated Femur Nail, Ctn-Cannulated Tibia Nail, Chn-Cannulated Humeral Nail

FDA 510(k) K132945 · I.T.S. GmbH

Substantially Equivalent

510(k) numberK132945

Submission

Device name
Cfn-Cannulated Femur Nail, Ctn-Cannulated Tibia Nail, Chn-Cannulated Humeral Nail
Applicant
I.T.S. GmbH
Prior Lake, MN, US
Received
September 19, 2013
Decision date
March 7, 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
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 Cfn-Cannulated Femur Nail, Ctn-Cannulated Tibia Nail, Chn-Cannulated Humeral Nail cleared by the FDA?

Cfn-Cannulated Femur Nail, Ctn-Cannulated Tibia Nail, Chn-Cannulated Humeral Nail (K132945) received a 510(k) decision of Substantially Equivalent on March 7, 2014, 169 days after the submission was received.

What is the product code of K132945?

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