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FDA 510(k)

TIGGES SPINAL

K-Number: K811176 · 1981-05-15

ApplicantThe Tiggs Co.
Decision Date1981-05-15
Product CodeIPW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TIGGES SPINAL is the device name listed in this FDA 510(k) record. The listed applicant is The Tiggs Co.. It received FDA 510(k) clearance on 1981-05-15 under 510(k) number K811176. The device is classified under product code IPW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIGGES SPINAL?

TIGGES SPINAL is a medical device that received FDA 510(k) clearance on 1981-05-15. The listed applicant is The Tiggs Co.. The 510(k) number is K811176.

When did TIGGES SPINAL receive FDA 510(k) clearance?

TIGGES SPINAL received FDA 510(k) clearance on 1981-05-15, under 510(k) number K811176.

Who is the listed applicant for TIGGES SPINAL?

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

What is the FDA product code for TIGGES SPINAL?

The FDA product code for TIGGES SPINAL is IPW.

Related Clinical Trials

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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