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FDA 510(k)

ACROMED CROSS ROD CONNECTOR

K-Number: K874882 · 1988-02-18

ApplicantAcromed Corp.
Decision Date1988-02-18
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACROMED CROSS ROD CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Acromed Corp.. It received FDA 510(k) clearance on 1988-02-18 under 510(k) number K874882. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACROMED CROSS ROD CONNECTOR?

ACROMED CROSS ROD CONNECTOR is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is Acromed Corp.. The 510(k) number is K874882.

When did ACROMED CROSS ROD CONNECTOR receive FDA 510(k) clearance?

ACROMED CROSS ROD CONNECTOR received FDA 510(k) clearance on 1988-02-18, under 510(k) number K874882.

Who is the listed applicant for ACROMED CROSS ROD CONNECTOR?

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

What is the FDA product code for ACROMED CROSS ROD CONNECTOR?

The FDA product code for ACROMED CROSS ROD CONNECTOR is KWP.

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 Acromed 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.

View all 41 devices →

Related Devices (Code: KWP)

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.

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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