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FDA 510(k)

INSERTEO, META.-PHAL.&THUMB CARPO-META

K-Number: K771072 · 1977-06-27

ApplicantDepuy, Inc.
Decision Date1977-06-27
Product CodeHXO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INSERTEO, META.-PHAL.&THUMB CARPO-META is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1977-06-27 under 510(k) number K771072. The device is classified under product code HXO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSERTEO, META.-PHAL.&THUMB CARPO-META?

INSERTEO, META.-PHAL.&THUMB CARPO-META is a medical device that received FDA 510(k) clearance on 1977-06-27. The listed applicant is Depuy, Inc.. The 510(k) number is K771072.

When did INSERTEO, META.-PHAL.&THUMB CARPO-META receive FDA 510(k) clearance?

INSERTEO, META.-PHAL.&THUMB CARPO-META received FDA 510(k) clearance on 1977-06-27, under 510(k) number K771072.

Who is the listed applicant for INSERTEO, META.-PHAL.&THUMB CARPO-META?

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 INSERTEO, META.-PHAL.&THUMB CARPO-META?

The FDA product code for INSERTEO, META.-PHAL.&THUMB CARPO-META is HXO.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: HXO)

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.

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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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