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FDA 510(k)

ORTHOPEDIC SPECIALTIES

K-Number: K770059 · 1977-01-14

Decision Date1977-01-14
Product Code
DecisionSubstantially Equivalent

Device Summary

ORTHOPEDIC SPECIALTIES is the device name listed in this FDA 510(k) record. The listed applicant is Robert R. Moore. It received FDA 510(k) clearance on 1977-01-14 under 510(k) number K770059. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOPEDIC SPECIALTIES?

ORTHOPEDIC SPECIALTIES is a medical device that received FDA 510(k) clearance on 1977-01-14. The listed applicant is Robert R. Moore. The 510(k) number is K770059.

When did ORTHOPEDIC SPECIALTIES receive FDA 510(k) clearance?

ORTHOPEDIC SPECIALTIES received FDA 510(k) clearance on 1977-01-14, under 510(k) number K770059.

Who is the listed applicant for ORTHOPEDIC SPECIALTIES?

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

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 Robert R. Moore 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.

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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