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FDA 510(k)

CREIGHTON FIXATOR

K-Number: K833907 · 1984-02-09

ApplicantPatton Machine Co.
Decision Date1984-02-09
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CREIGHTON FIXATOR is the device name listed in this FDA 510(k) record. The listed applicant is Patton Machine Co.. It received FDA 510(k) clearance on 1984-02-09 under 510(k) number K833907. 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 CREIGHTON FIXATOR?

CREIGHTON FIXATOR is a medical device that received FDA 510(k) clearance on 1984-02-09. The listed applicant is Patton Machine Co.. The 510(k) number is K833907.

When did CREIGHTON FIXATOR receive FDA 510(k) clearance?

CREIGHTON FIXATOR received FDA 510(k) clearance on 1984-02-09, under 510(k) number K833907.

Who is the listed applicant for CREIGHTON FIXATOR?

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

What is the FDA product code for CREIGHTON FIXATOR?

The FDA product code for CREIGHTON FIXATOR is JDW.

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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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