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FDA 510(k)

ORTHOPEDIC IMPLANT NAILS & PINS

K-Number: K850026 · 1985-05-20

ApplicantKirkstil Corp., Inc.
Decision Date1985-05-20
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ORTHOPEDIC IMPLANT NAILS & PINS is the device name listed in this FDA 510(k) record. The listed applicant is Kirkstil Corp., Inc.. It received FDA 510(k) clearance on 1985-05-20 under 510(k) number K850026. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOPEDIC IMPLANT NAILS & PINS?

ORTHOPEDIC IMPLANT NAILS & PINS is a medical device that received FDA 510(k) clearance on 1985-05-20. The listed applicant is Kirkstil Corp., Inc.. The 510(k) number is K850026.

When did ORTHOPEDIC IMPLANT NAILS & PINS receive FDA 510(k) clearance?

ORTHOPEDIC IMPLANT NAILS & PINS received FDA 510(k) clearance on 1985-05-20, under 510(k) number K850026.

Who is the listed applicant for ORTHOPEDIC IMPLANT NAILS & PINS?

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

What is the FDA product code for ORTHOPEDIC IMPLANT NAILS & PINS?

The FDA product code for ORTHOPEDIC IMPLANT NAILS & PINS is HTY.

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.

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Other records listing Kirkstil Corp., 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.

K850025ORTHOPEDIC IMPLANT PLATESK850024ORTHOPEDIC IMPLANT SCREWS

Related Devices (Code: HTY)

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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