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FDA 510(k)

PARTIALLY THREADED BONE FIX. PIN

K-Number: K842293 · 1984-08-02

ApplicantWarsaw Orthopedic, Inc.
Decision Date1984-08-02
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PARTIALLY THREADED BONE FIX. PIN is the device name listed in this FDA 510(k) record. The listed applicant is Warsaw Orthopedic, Inc.. It received FDA 510(k) clearance on 1984-08-02 under 510(k) number K842293. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARTIALLY THREADED BONE FIX. PIN?

PARTIALLY THREADED BONE FIX. PIN is a medical device that received FDA 510(k) clearance on 1984-08-02. The listed applicant is Warsaw Orthopedic, Inc.. The 510(k) number is K842293.

When did PARTIALLY THREADED BONE FIX. PIN receive FDA 510(k) clearance?

PARTIALLY THREADED BONE FIX. PIN received FDA 510(k) clearance on 1984-08-02, under 510(k) number K842293.

Who is the listed applicant for PARTIALLY THREADED BONE FIX. PIN?

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

What is the FDA product code for PARTIALLY THREADED BONE FIX. PIN?

The FDA product code for PARTIALLY THREADED BONE FIX. PIN is JDW.

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Other records listing Warsaw Orthopedic, 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.

K892877CRADLE, HOSPITAL BED CLOTHINGK883783TSRH SACRAL SPINAL SCREWK883784TSRH ANTERIOR SPINAL SCREWS, STAPLES AND END PLATEK880211TSRH H/M HOOK HOLDERK880212TSRH H/M HOOK HOLDER W/ROD MOVERK880215TSRH H/M HOOK, EYEBOLT/LOCK NUT ASSEM., SPINAL ROD

View all 24 devices →

Related Devices (Code: JDW)

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.

K260073XT3 System; XT3 System, Mini; XT3 System, 40mm; XT3 System, Mini, 40mmBiodynamik, Inc.K250316Meduloc Intramedullary Fracture Fixation (IFF) SystemMeduloc, LLCK241357XT3 SystemBiodynamik, Inc.K223112MAVERICK Mini External Fixation SystemSmith & Nephew, Inc.K213874MAVERICK External Fixation SystemSmith & Nephew, Inc.K211508Steinmann Pins and Kirschner WiresStryker GmbH

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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