Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VERTEBRACE SPINAL SUPPORTS

K-Number: K791314 · 1979-07-30

Decision Date1979-07-30
Product CodeIPY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VERTEBRACE SPINAL SUPPORTS is the device name listed in this FDA 510(k) record. The listed applicant is Vertebrace, Inc.. It received FDA 510(k) clearance on 1979-07-30 under 510(k) number K791314. The device is classified under product code IPY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERTEBRACE SPINAL SUPPORTS?

VERTEBRACE SPINAL SUPPORTS is a medical device that received FDA 510(k) clearance on 1979-07-30. The listed applicant is Vertebrace, Inc.. The 510(k) number is K791314.

When did VERTEBRACE SPINAL SUPPORTS receive FDA 510(k) clearance?

VERTEBRACE SPINAL SUPPORTS received FDA 510(k) clearance on 1979-07-30, under 510(k) number K791314.

Who is the listed applicant for VERTEBRACE SPINAL SUPPORTS?

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

What is the FDA product code for VERTEBRACE SPINAL SUPPORTS?

The FDA product code for VERTEBRACE SPINAL SUPPORTS is IPY.

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.

Related Devices (Code: IPY)

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.

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.

↑