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FDA 510(k)

CORTICAL BONE SCREWS

K-Number: K872738 · 1987-07-30

ApplicantMilitary Engineering, Inc.
Decision Date1987-07-30
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CORTICAL BONE SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Military Engineering, Inc.. It received FDA 510(k) clearance on 1987-07-30 under 510(k) number K872738. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORTICAL BONE SCREWS?

CORTICAL BONE SCREWS is a medical device that received FDA 510(k) clearance on 1987-07-30. The listed applicant is Military Engineering, Inc.. The 510(k) number is K872738.

When did CORTICAL BONE SCREWS receive FDA 510(k) clearance?

CORTICAL BONE SCREWS received FDA 510(k) clearance on 1987-07-30, under 510(k) number K872738.

Who is the listed applicant for CORTICAL BONE SCREWS?

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

What is the FDA product code for CORTICAL BONE SCREWS?

The FDA product code for CORTICAL BONE SCREWS is HWC. This falls under the Cardiovascular category.

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Other records listing Military Engineering, 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.

K874335EXPLORER-DENTAL PROBERK873715BONE PIN CUTTER 18K872842PIN, HIP, KNOWLESK871834DRILL, HAND, BONE, SMEDBERGK872091CURRETTES, ALVEOLAR (MOLT AND MILLER)K872609CURETTE SET, ANTRUM, COAKLEY

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Related Devices (Code: HWC)

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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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