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FDA 510(k)

ISOLA(R) TRANSVERSE ROD DUAL CONNECTOR

K-Number: K921090 · 1992-12-31

ApplicantAcromed Corp.
Decision Date1992-12-31
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ISOLA(R) TRANSVERSE ROD DUAL 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 1992-12-31 under 510(k) number K921090. 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 ISOLA(R) TRANSVERSE ROD DUAL CONNECTOR?

ISOLA(R) TRANSVERSE ROD DUAL CONNECTOR is a medical device that received FDA 510(k) clearance on 1992-12-31. The listed applicant is Acromed Corp.. The 510(k) number is K921090.

When did ISOLA(R) TRANSVERSE ROD DUAL CONNECTOR receive FDA 510(k) clearance?

ISOLA(R) TRANSVERSE ROD DUAL CONNECTOR received FDA 510(k) clearance on 1992-12-31, under 510(k) number K921090.

Who is the listed applicant for ISOLA(R) TRANSVERSE ROD DUAL 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 ISOLA(R) TRANSVERSE ROD DUAL CONNECTOR?

The FDA product code for ISOLA(R) TRANSVERSE ROD DUAL CONNECTOR is KWP.

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Other records listing Acromed Corp. as applicant

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Related Devices (Code: KWP)

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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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