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FDA 510(k)

PIN HOLDERS, TRANSFIXING PINS, OL WIRES, HALF PINS

K-Number: K932853 · 1994-02-22

Decision Date1994-02-22
Product CodeJEL
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PIN HOLDERS, TRANSFIXING PINS, OL WIRES, HALF PINS is the device name listed in this FDA 510(k) record. The listed applicant is Applied Osteo Systems, Inc.. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K932853. The device is classified under product code JEL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIN HOLDERS, TRANSFIXING PINS, OL WIRES, HALF PINS?

PIN HOLDERS, TRANSFIXING PINS, OL WIRES, HALF PINS is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Applied Osteo Systems, Inc.. The 510(k) number is K932853.

When did PIN HOLDERS, TRANSFIXING PINS, OL WIRES, HALF PINS receive FDA 510(k) clearance?

PIN HOLDERS, TRANSFIXING PINS, OL WIRES, HALF PINS received FDA 510(k) clearance on 1994-02-22, under 510(k) number K932853.

Who is the listed applicant for PIN HOLDERS, TRANSFIXING PINS, OL WIRES, HALF PINS?

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

What is the FDA product code for PIN HOLDERS, TRANSFIXING PINS, OL WIRES, HALF PINS?

The FDA product code for PIN HOLDERS, TRANSFIXING PINS, OL WIRES, HALF PINS is JEL.

Related Clinical Trials

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.

Other records listing Applied Osteo Systems, 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.

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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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