FDA 510(k)

RAYLOR(TM) OSTEOTOMES

K-Number: K864423 · 1986-11-24

Decision Date1986-11-24

Product Code

DecisionSubstantially Equivalent

Device Summary

RAYLOR(TM) OSTEOTOMES 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 1986-11-24 under 510(k) number K864423. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAYLOR(TM) OSTEOTOMES?

RAYLOR(TM) OSTEOTOMES is a medical device that received FDA 510(k) clearance on 1986-11-24. The listed applicant is Cedar Surgical, Inc.. The 510(k) number is K864423.

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

RAYLOR(TM) OSTEOTOMES received FDA 510(k) clearance on 1986-11-24, under 510(k) number K864423.

Who is the listed applicant for RAYLOR(TM) OSTEOTOMES?

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

Related Clinical Trials

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Other records listing Cedar Surgical, Inc. as applicant

K873692RAYLOR(TM) DRILL STOP K872281RAYLOR FUSION FUNNEL K873690CEDAR(TM) PELVIC CUSHION K873691CEDAR(TM) RETRACTOR RING K864425RAYLOR(TM) DISSECTING HOOK K864426RAYLOR(TM) DEPTH GAUGE

View all 17 devices →

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.