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FDA 510(k)

OVERLOAD WARNING DEVICE

K-Number: K770405 · 1977-03-10

ApplicantSynthes (Usa)
Decision Date1977-03-10
Product CodeIRN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

OVERLOAD WARNING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 1977-03-10 under 510(k) number K770405. The device is classified under product code IRN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OVERLOAD WARNING DEVICE?

OVERLOAD WARNING DEVICE is a medical device that received FDA 510(k) clearance on 1977-03-10. The listed applicant is Synthes (Usa). The 510(k) number is K770405.

When did OVERLOAD WARNING DEVICE receive FDA 510(k) clearance?

OVERLOAD WARNING DEVICE received FDA 510(k) clearance on 1977-03-10, under 510(k) number K770405.

Who is the listed applicant for OVERLOAD WARNING DEVICE?

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

What is the FDA product code for OVERLOAD WARNING DEVICE?

The FDA product code for OVERLOAD WARNING DEVICE is IRN.

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Other records listing Synthes (Usa) as applicant

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Related Devices (Code: IRN)

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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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