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FDA 510(k)

SLOT STAPLES AND ADAPTOR FOR ZIELKE SPINAL FIXATIO

K-Number: K897141 · 1990-06-21

ApplicantStuart
Decision Date1990-06-21
Product CodeJDN
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

SLOT STAPLES AND ADAPTOR FOR ZIELKE SPINAL FIXATIO is the device name listed in this FDA 510(k) record. The listed applicant is Stuart. It received FDA 510(k) clearance on 1990-06-21 under 510(k) number K897141. The device is classified under product code JDN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the SLOT STAPLES AND ADAPTOR FOR ZIELKE SPINAL FIXATIO?

SLOT STAPLES AND ADAPTOR FOR ZIELKE SPINAL FIXATIO is a medical device that received FDA 510(k) clearance on 1990-06-21. The listed applicant is Stuart. The 510(k) number is K897141.

When did SLOT STAPLES AND ADAPTOR FOR ZIELKE SPINAL FIXATIO receive FDA 510(k) clearance?

SLOT STAPLES AND ADAPTOR FOR ZIELKE SPINAL FIXATIO received FDA 510(k) clearance on 1990-06-21, under 510(k) number K897141.

Who is the listed applicant for SLOT STAPLES AND ADAPTOR FOR ZIELKE SPINAL FIXATIO?

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

What is the FDA product code for SLOT STAPLES AND ADAPTOR FOR ZIELKE SPINAL FIXATIO?

The FDA product code for SLOT STAPLES AND ADAPTOR FOR ZIELKE SPINAL FIXATIO is JDN.

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 Stuart 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.

Related Devices (Code: JDN)

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

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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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