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FDA 510(k)

RAYLOR(TM) PERIOSTEAL ELEVATORS

K-Number: K864421 · 1986-11-26

Decision Date1986-11-26
Product CodeGEG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RAYLOR(TM) PERIOSTEAL ELEVATORS is the device name listed in this FDA 510(k) record. The listed applicant is Cedar Surgical, Inc.. It received FDA 510(k) clearance on 1986-11-26 under 510(k) number K864421. The device is classified under product code GEG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAYLOR(TM) PERIOSTEAL ELEVATORS?

RAYLOR(TM) PERIOSTEAL ELEVATORS is a medical device that received FDA 510(k) clearance on 1986-11-26. The listed applicant is Cedar Surgical, Inc.. The 510(k) number is K864421.

When did RAYLOR(TM) PERIOSTEAL ELEVATORS receive FDA 510(k) clearance?

RAYLOR(TM) PERIOSTEAL ELEVATORS received FDA 510(k) clearance on 1986-11-26, under 510(k) number K864421.

Who is the listed applicant for RAYLOR(TM) PERIOSTEAL ELEVATORS?

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

What is the FDA product code for RAYLOR(TM) PERIOSTEAL ELEVATORS?

The FDA product code for RAYLOR(TM) PERIOSTEAL ELEVATORS is GEG.

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.

Other records listing Cedar Surgical, Inc. 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.

View all 17 devices →

Related Devices (Code: GEG)

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

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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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