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FDA 510(k)

CHARNLEY FEMUR DRILL #1 AND #2

K-Number: K760977 · 1976-11-16

ApplicantCodman & Shurtleff, Inc.
Decision Date1976-11-16
Product CodeHWE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CHARNLEY FEMUR DRILL #1 AND #2 is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1976-11-16 under 510(k) number K760977. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHARNLEY FEMUR DRILL #1 AND #2?

CHARNLEY FEMUR DRILL #1 AND #2 is a medical device that received FDA 510(k) clearance on 1976-11-16. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K760977.

When did CHARNLEY FEMUR DRILL #1 AND #2 receive FDA 510(k) clearance?

CHARNLEY FEMUR DRILL #1 AND #2 received FDA 510(k) clearance on 1976-11-16, under 510(k) number K760977.

Who is the listed applicant for CHARNLEY FEMUR DRILL #1 AND #2?

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

What is the FDA product code for CHARNLEY FEMUR DRILL #1 AND #2?

The FDA product code for CHARNLEY FEMUR DRILL #1 AND #2 is HWE.

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Related Devices (Code: HWE)

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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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