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FDA 510(k)

MIAMI, PROTRUSIO RING

K-Number: K812182 · 1981-08-18

ApplicantZimmer, Inc.
Decision Date1981-08-18
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MIAMI, PROTRUSIO RING is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1981-08-18 under 510(k) number K812182. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIAMI, PROTRUSIO RING?

MIAMI, PROTRUSIO RING is a medical device that received FDA 510(k) clearance on 1981-08-18. The listed applicant is Zimmer, Inc.. The 510(k) number is K812182.

When did MIAMI, PROTRUSIO RING receive FDA 510(k) clearance?

MIAMI, PROTRUSIO RING received FDA 510(k) clearance on 1981-08-18, under 510(k) number K812182.

Who is the listed applicant for MIAMI, PROTRUSIO RING?

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 MIAMI, PROTRUSIO RING?

The FDA product code for MIAMI, PROTRUSIO RING is JDI.

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Related Devices (Code: JDI)

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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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