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FDA 510(k)

Pediatric Nailing Platform Femur

K-Number: K220679 · 2022-07-20

ApplicantOrthoPediatrics Corp.
Decision Date2022-07-20
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Pediatric Nailing Platform Femur is the device name listed in this FDA 510(k) record. The listed applicant is OrthoPediatrics Corp.. It received FDA 510(k) clearance on 2022-07-20 under 510(k) number K220679. 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 Pediatric Nailing Platform Femur?

Pediatric Nailing Platform Femur is a medical device that received FDA 510(k) clearance on 2022-07-20. The listed applicant is OrthoPediatrics Corp.. The 510(k) number is K220679.

When did Pediatric Nailing Platform Femur receive FDA 510(k) clearance?

Pediatric Nailing Platform Femur received FDA 510(k) clearance on 2022-07-20, under 510(k) number K220679.

Who is the listed applicant for Pediatric Nailing Platform Femur?

The FDA 510(k) record lists OrthoPediatrics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Pediatric Nailing Platform Femur?

The FDA product code for Pediatric Nailing Platform Femur is HSB.

Other records listing OrthoPediatrics Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260323OrthoPediatrics® Locking Cannulated Blade Plate SystemK252600Pediatric Plating Platform I Small-MiniK251362PediFlex™ Flexible Nail SystemK243963Pediatric Plating Platform HipK250623Pediatric Nailing Platform Tibia Pediatric Nailing Platform FemurK241816VerteGlide Spinal Growth Guidance System

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Related Devices (Code: HSB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261481Pangea Femur Reconstruction SystemStryker GmbHK261651Precice™ Max System and Precice™ Ankle Salvage SystemNuVasive Specialized OrthopedicsK253080AND Medical Femoral Nail System (PFNA01); AND Medical Femoral Nail System (PFNA02)Suzhou and Science & Technology Development Corp.K253155Fule Metallic Lockable Intramedullary Nail SystemsBeijing Fule Science & Technology Development Co., Ltd.K253046HERA Interlocking Intramedullary Nailing SystemZheJiang Decans Medical Devices Co., Ltd.K260146FITBONE® TRANSPORT AND LENGTHENING SYSTEMOrthofix Srl

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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