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FDA 510(k)

FORCEPS, ANKLE INSERTING, CON-AXIAL

K-Number: K770420 · 1977-03-14

ApplicantDepuy, Inc.
Decision Date1977-03-14
Product CodeHSN
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FORCEPS, ANKLE INSERTING, CON-AXIAL is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1977-03-14 under 510(k) number K770420. The device is classified under product code HSN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCEPS, ANKLE INSERTING, CON-AXIAL?

FORCEPS, ANKLE INSERTING, CON-AXIAL is a medical device that received FDA 510(k) clearance on 1977-03-14. The listed applicant is Depuy, Inc.. The 510(k) number is K770420.

When did FORCEPS, ANKLE INSERTING, CON-AXIAL receive FDA 510(k) clearance?

FORCEPS, ANKLE INSERTING, CON-AXIAL received FDA 510(k) clearance on 1977-03-14, under 510(k) number K770420.

Who is the listed applicant for FORCEPS, ANKLE INSERTING, CON-AXIAL?

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 FORCEPS, ANKLE INSERTING, CON-AXIAL?

The FDA product code for FORCEPS, ANKLE INSERTING, CON-AXIAL is HSN.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: HSN)

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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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