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FDA 510(k)

INTRAMEDULLARY ROD

K-Number: K830087 · 1983-03-01

ApplicantThe Deca Co.
Decision Date1983-03-01
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTRAMEDULLARY ROD is the device name listed in this FDA 510(k) record. The listed applicant is The Deca Co.. It received FDA 510(k) clearance on 1983-03-01 under 510(k) number K830087. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRAMEDULLARY ROD?

INTRAMEDULLARY ROD is a medical device that received FDA 510(k) clearance on 1983-03-01. The listed applicant is The Deca Co.. The 510(k) number is K830087.

When did INTRAMEDULLARY ROD receive FDA 510(k) clearance?

INTRAMEDULLARY ROD received FDA 510(k) clearance on 1983-03-01, under 510(k) number K830087.

Who is the listed applicant for INTRAMEDULLARY ROD?

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

What is the FDA product code for INTRAMEDULLARY ROD?

The FDA product code for INTRAMEDULLARY ROD is HSB.

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Other records listing The Deca Co. 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.

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Related Devices (Code: HSB)

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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