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FDA 510(k)

KIRSCHNER ORTHOPEDIC WIRE, EYELET CERCLAGE WIRES

K-Number: K850631 · 1985-05-01

ApplicantKirschner Medical Corp.
Decision Date1985-05-01
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KIRSCHNER ORTHOPEDIC WIRE, EYELET CERCLAGE WIRES is the device name listed in this FDA 510(k) record. The listed applicant is Kirschner Medical Corp.. It received FDA 510(k) clearance on 1985-05-01 under 510(k) number K850631. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIRSCHNER ORTHOPEDIC WIRE, EYELET CERCLAGE WIRES?

KIRSCHNER ORTHOPEDIC WIRE, EYELET CERCLAGE WIRES is a medical device that received FDA 510(k) clearance on 1985-05-01. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K850631.

When did KIRSCHNER ORTHOPEDIC WIRE, EYELET CERCLAGE WIRES receive FDA 510(k) clearance?

KIRSCHNER ORTHOPEDIC WIRE, EYELET CERCLAGE WIRES received FDA 510(k) clearance on 1985-05-01, under 510(k) number K850631.

Who is the listed applicant for KIRSCHNER ORTHOPEDIC WIRE, EYELET CERCLAGE WIRES?

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

What is the FDA product code for KIRSCHNER ORTHOPEDIC WIRE, EYELET CERCLAGE WIRES?

The FDA product code for KIRSCHNER ORTHOPEDIC WIRE, EYELET CERCLAGE WIRES is JDQ.

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Other records listing Kirschner Medical 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.

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Related Devices (Code: JDQ)

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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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