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FDA 510(k)

DePuy Synthes Retrograde Femoral Nail Advanced System

K-Number: K233696 · 2024-08-01

ApplicantDePuy Synthes
Decision Date2024-08-01
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DePuy Synthes Retrograde Femoral Nail Advanced System is a medical device manufactured by DePuy Synthes. It received FDA 510(k) clearance on 2024-08-01 under approval number K233696. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DePuy Synthes Retrograde Femoral Nail Advanced System?

DePuy Synthes Retrograde Femoral Nail Advanced System is a medical device that received FDA 510(k) clearance on 2024-08-01. It is manufactured by DePuy Synthes. The 510(k) number is K233696.

When was DePuy Synthes Retrograde Femoral Nail Advanced System approved by the FDA?

DePuy Synthes Retrograde Femoral Nail Advanced System received FDA 510(k) clearance on 2024-08-01, under approval number K233696.

What company makes DePuy Synthes Retrograde Femoral Nail Advanced System?

DePuy Synthes Retrograde Femoral Nail Advanced System is manufactured by DePuy Synthes.

What is the FDA product code for DePuy Synthes Retrograde Femoral Nail Advanced System?

The FDA product code for DePuy Synthes Retrograde Femoral Nail Advanced System is HSB.

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Other Devices by DePuy Synthes

K162124Synthes 4.5mm VA-LCP Curved Condylar Plate System Line Extension, Variable Angle Positioning Pins K163046DePuy Synthes 2.4/2.7mm VA LCP Two-Column Volar Distal Radius Plate, Extra-Long K182783DePuy Synthes Trauma Orthopedic Nail Implants K172872DePuy Synthes Femoral Neck System K190750DePuy Synthes Plates and Screws Portfolio K190409MatrixRIB Fixation System

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Related Devices (Code: HSB)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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