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FDA 510(k)

NUVA-COTE (MODIFICATION TO)

K-Number: K771402 · 1977-08-26

ApplicantL.D. Caulk Co.
Decision Date1977-08-26
Product CodeEBC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NUVA-COTE (MODIFICATION TO) is the device name listed in this FDA 510(k) record. The listed applicant is L.D. Caulk Co.. It received FDA 510(k) clearance on 1977-08-26 under 510(k) number K771402. The device is classified under product code EBC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUVA-COTE (MODIFICATION TO)?

NUVA-COTE (MODIFICATION TO) is a medical device that received FDA 510(k) clearance on 1977-08-26. The listed applicant is L.D. Caulk Co.. The 510(k) number is K771402.

When did NUVA-COTE (MODIFICATION TO) receive FDA 510(k) clearance?

NUVA-COTE (MODIFICATION TO) received FDA 510(k) clearance on 1977-08-26, under 510(k) number K771402.

Who is the listed applicant for NUVA-COTE (MODIFICATION TO)?

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

What is the FDA product code for NUVA-COTE (MODIFICATION TO)?

The FDA product code for NUVA-COTE (MODIFICATION TO) is EBC.

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Other records listing L.D. Caulk 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 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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