FDA 510(k)

INTRAMEDULLARY ROD

K-Number: K861183 · 1986-08-11

Decision Date1986-08-11

Product Code

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 1986-08-11 under 510(k) number K861183. 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 1986-08-11. The listed applicant is The Deca Co.. The 510(k) number is K861183.

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

INTRAMEDULLARY ROD received FDA 510(k) clearance on 1986-08-11, under 510(k) number K861183.

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.

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Other records listing The Deca Co. as applicant

K870041FLEXIBLE FASCICULATED BONE PLATE K870040INTRAMEDULLARY NAIL K863215FASCICULATED I ROD K863271FASCICULATED S ROD K863239FASCICULATED BOAT ROD K854227FASCILULATED NAIL

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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.