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FDA 510(k)

MODULAR CONSTRUCT FRAME EXTERNAL FIXA

K-Number: K840856 · 1984-04-25

ApplicantPrecision Medical Devices, Inc.
Decision Date1984-04-25
Product CodeJEC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODULAR CONSTRUCT FRAME EXTERNAL FIXA is the device name listed in this FDA 510(k) record. The listed applicant is Precision Medical Devices, Inc.. It received FDA 510(k) clearance on 1984-04-25 under 510(k) number K840856. The device is classified under product code JEC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODULAR CONSTRUCT FRAME EXTERNAL FIXA?

MODULAR CONSTRUCT FRAME EXTERNAL FIXA is a medical device that received FDA 510(k) clearance on 1984-04-25. The listed applicant is Precision Medical Devices, Inc.. The 510(k) number is K840856.

When did MODULAR CONSTRUCT FRAME EXTERNAL FIXA receive FDA 510(k) clearance?

MODULAR CONSTRUCT FRAME EXTERNAL FIXA received FDA 510(k) clearance on 1984-04-25, under 510(k) number K840856.

Who is the listed applicant for MODULAR CONSTRUCT FRAME EXTERNAL FIXA?

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

What is the FDA product code for MODULAR CONSTRUCT FRAME EXTERNAL FIXA?

The FDA product code for MODULAR CONSTRUCT FRAME EXTERNAL FIXA is JEC.

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Other records listing Precision Medical Devices, Inc. as applicant

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Related Devices (Code: JEC)

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Official Source

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

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