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FDA 510(k)

PROM NAID

K-Number: K843581 · 1984-12-11

ApplicantLossing Orthopedic, Inc.
Decision Date1984-12-11
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PROM NAID is the device name listed in this FDA 510(k) record. The listed applicant is Lossing Orthopedic, Inc.. It received FDA 510(k) clearance on 1984-12-11 under 510(k) number K843581. The device is classified under product code ITH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROM NAID?

PROM NAID is a medical device that received FDA 510(k) clearance on 1984-12-11. The listed applicant is Lossing Orthopedic, Inc.. The 510(k) number is K843581.

When did PROM NAID receive FDA 510(k) clearance?

PROM NAID received FDA 510(k) clearance on 1984-12-11, under 510(k) number K843581.

Who is the listed applicant for PROM NAID?

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

What is the FDA product code for PROM NAID?

The FDA product code for PROM NAID is ITH.

Other records listing Lossing Orthopedic, Inc. as applicant

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Related Devices (Code: ITH)

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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