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FDA 510(k)

DRLOCK DISTAL RADIUS VOLAR SYSTEM

K-Number: K053182 · 2006-02-27

ApplicantOrthohelix Surgical Designs, Inc.
Decision Date2006-02-27
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DRLOCK DISTAL RADIUS VOLAR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Orthohelix Surgical Designs, Inc.. It received FDA 510(k) clearance on 2006-02-27 under 510(k) number K053182. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRLOCK DISTAL RADIUS VOLAR SYSTEM?

DRLOCK DISTAL RADIUS VOLAR SYSTEM is a medical device that received FDA 510(k) clearance on 2006-02-27. The listed applicant is Orthohelix Surgical Designs, Inc.. The 510(k) number is K053182.

When did DRLOCK DISTAL RADIUS VOLAR SYSTEM receive FDA 510(k) clearance?

DRLOCK DISTAL RADIUS VOLAR SYSTEM received FDA 510(k) clearance on 2006-02-27, under 510(k) number K053182.

Who is the listed applicant for DRLOCK DISTAL RADIUS VOLAR SYSTEM?

The FDA 510(k) record lists Orthohelix Surgical Designs, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRLOCK DISTAL RADIUS VOLAR SYSTEM?

The FDA product code for DRLOCK DISTAL RADIUS VOLAR SYSTEM is HRS.

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Other records listing Orthohelix Surgical Designs, Inc. 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.

K132591MAXLOCK EXTREME SYSTEMK130832ORTHOHELIX STAPLE SYSTEMK131324MAXTORQUE SCREW SYSTEMK123203MAXLOCK EXTREME SYSTEM MODEL MXLK122005MAXLOCK EXTREME SYSTEMK121437MINI MAXLOCK EXTREME PLATING SYSTEM

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Related Devices (Code: HRS)

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.

K261892ProRib Fixation SystemCosta Surgical, Inc.K262098EnHAnce PEEK Bunion SystemNvision Biomedical TechnologiesK262963TMC Implant Fixation SystemTreace Medical Concepts, Inc.K261647Tempo Plating System; Ultra Compression Screw SystemPace SurgicalK261830FRAXION 3.5 Plate System (Various - See Catalog);FRAXION 4.5 Plate System (Various - See Catalog);FRAXION Mini Plate System (Various - See Catalog);FRAXION Bone Screw System (Various - See Catalog)Ortler Global Tibbi Gerecler Anonim SirketiK262537Versalock Sterile Plating SystemGM Dos Reis Industria e Comercio Ltda.

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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