Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SPINAL SURGERY INSTRUMENTATION

K-Number: K782061 · 1979-03-21

Decision Date1979-03-21
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SPINAL SURGERY INSTRUMENTATION is the device name listed in this FDA 510(k) record. The listed applicant is Stuart Drug & Surgical Supply, Inc.. It received FDA 510(k) clearance on 1979-03-21 under 510(k) number K782061. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPINAL SURGERY INSTRUMENTATION?

SPINAL SURGERY INSTRUMENTATION is a medical device that received FDA 510(k) clearance on 1979-03-21. The listed applicant is Stuart Drug & Surgical Supply, Inc.. The 510(k) number is K782061.

When did SPINAL SURGERY INSTRUMENTATION receive FDA 510(k) clearance?

SPINAL SURGERY INSTRUMENTATION received FDA 510(k) clearance on 1979-03-21, under 510(k) number K782061.

Who is the listed applicant for SPINAL SURGERY INSTRUMENTATION?

The FDA 510(k) record lists Stuart Drug & Surgical Supply, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPINAL SURGERY INSTRUMENTATION?

The FDA product code for SPINAL SURGERY INSTRUMENTATION is KWQ.

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 Drug & Surgical Supply, 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.

Related Devices (Code: KWQ)

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.

↑