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FDA 510(k)

RASPS FOR SCRAPING BONE

K-Number: K771745 · 1977-09-28

ApplicantDepuy, Inc.
Decision Date1977-09-28
Product CodeHTR
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RASPS FOR SCRAPING BONE is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1977-09-28 under 510(k) number K771745. The device is classified under product code HTR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RASPS FOR SCRAPING BONE?

RASPS FOR SCRAPING BONE is a medical device that received FDA 510(k) clearance on 1977-09-28. The listed applicant is Depuy, Inc.. The 510(k) number is K771745.

When did RASPS FOR SCRAPING BONE receive FDA 510(k) clearance?

RASPS FOR SCRAPING BONE received FDA 510(k) clearance on 1977-09-28, under 510(k) number K771745.

Who is the listed applicant for RASPS FOR SCRAPING BONE?

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

What is the FDA product code for RASPS FOR SCRAPING BONE?

The FDA product code for RASPS FOR SCRAPING BONE is HTR.

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 Depuy, 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.

View all 303 devices →

Related Devices (Code: HTR)

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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