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FDA 510(k)

HOFFMANN II CARBON CONNECTING ROD

K-Number: K961916 · 1996-08-01

Decision Date1996-08-01
Product CodeJEC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HOFFMANN II CARBON CONNECTING ROD is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica, Inc.. It received FDA 510(k) clearance on 1996-08-01 under 510(k) number K961916. The device is classified under product code JEC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOFFMANN II CARBON CONNECTING ROD?

HOFFMANN II CARBON CONNECTING ROD is a medical device that received FDA 510(k) clearance on 1996-08-01. The listed applicant is Howmedica, Inc.. The 510(k) number is K961916.

When did HOFFMANN II CARBON CONNECTING ROD receive FDA 510(k) clearance?

HOFFMANN II CARBON CONNECTING ROD received FDA 510(k) clearance on 1996-08-01, under 510(k) number K961916.

Who is the listed applicant for HOFFMANN II CARBON CONNECTING ROD?

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

What is the FDA product code for HOFFMANN II CARBON CONNECTING ROD?

The FDA product code for HOFFMANN II CARBON CONNECTING ROD is JEC.

Related Clinical Trials

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.

Other records listing Howmedica, Inc. as applicant

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.

View all 36 devices →

Related Devices (Code: JEC)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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