FDA 510(k)

FASCICULATED S ROD

K-Number: K863271 · 1986-12-24

Decision Date1986-12-24

Product Code

DecisionSubstantially Equivalent

Device Summary

FASCICULATED S 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 1986-12-24 under 510(k) number K863271. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FASCICULATED S ROD?

FASCICULATED S ROD is a medical device that received FDA 510(k) clearance on 1986-12-24. The listed applicant is The Deca Co.. The 510(k) number is K863271.

When did FASCICULATED S ROD receive FDA 510(k) clearance?

FASCICULATED S ROD received FDA 510(k) clearance on 1986-12-24, under 510(k) number K863271.

Who is the listed applicant for FASCICULATED S 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 K863239FASCICULATED BOAT ROD K863215FASCICULATED I ROD K861183INTRAMEDULLARY 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.