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FDA 510(k)

ORHTOPEDIC REAMER 87 HTD

K-Number: K802676 · 1980-11-12

ApplicantZimmer, Inc.
Decision Date1980-11-12
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ORHTOPEDIC REAMER 87 HTD is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802676. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORHTOPEDIC REAMER 87 HTD?

ORHTOPEDIC REAMER 87 HTD is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Zimmer, Inc.. The 510(k) number is K802676.

When did ORHTOPEDIC REAMER 87 HTD receive FDA 510(k) clearance?

ORHTOPEDIC REAMER 87 HTD received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802676.

Who is the listed applicant for ORHTOPEDIC REAMER 87 HTD?

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

What is the FDA product code for ORHTOPEDIC REAMER 87 HTD?

The FDA product code for ORHTOPEDIC REAMER 87 HTD is HTD.

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Related Devices (Code: HTD)

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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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