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FDA 510(k)

OSTEOTOMES FOR CUTTING BONH

K-Number: K771744 · 1977-09-28

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

Device Summary

OSTEOTOMES FOR CUTTING BONH 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 K771744. The device is classified under product code HWM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSTEOTOMES FOR CUTTING BONH?

OSTEOTOMES FOR CUTTING BONH 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 K771744.

When did OSTEOTOMES FOR CUTTING BONH receive FDA 510(k) clearance?

OSTEOTOMES FOR CUTTING BONH received FDA 510(k) clearance on 1977-09-28, under 510(k) number K771744.

Who is the listed applicant for OSTEOTOMES FOR CUTTING BONH?

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 OSTEOTOMES FOR CUTTING BONH?

The FDA product code for OSTEOTOMES FOR CUTTING BONH is HWM.

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Related Devices (Code: HWM)

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.

K874503MICRO-AIRE OSTEOTOME SYSTEM OR BONE HARVESTERMicro-Aire Surgical Instruments, Inc.K870780ACROMED WALLIE-HEINIG OSTEOTOMESBuckman Co., Inc.

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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