FDA 510(k)

KSF SPINAL FIXATOR

K-Number: K931488 · 1994-01-21

Decision Date1994-01-21

Product Code

DecisionSubstantially Equivalent for Some Indications

Device Summary

KSF SPINAL FIXATOR is the device name listed in this FDA 510(k) record. The listed applicant is Franklin Medical USA, Inc.. It received FDA 510(k) clearance on 1994-01-21 under 510(k) number K931488. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the KSF SPINAL FIXATOR?

KSF SPINAL FIXATOR is a medical device that received FDA 510(k) clearance on 1994-01-21. The listed applicant is Franklin Medical USA, Inc.. The 510(k) number is K931488.

When did KSF SPINAL FIXATOR receive FDA 510(k) clearance?

KSF SPINAL FIXATOR received FDA 510(k) clearance on 1994-01-21, under 510(k) number K931488.

Who is the listed applicant for KSF SPINAL FIXATOR?

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

Related Clinical Trials

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Other records listing Franklin Medical USA, Inc. as applicant

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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.