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FDA 510(k)

RAYLOR BONE IMPACTORS

K-Number: K863415 · 1986-09-24

ApplicantCedar Surgical, Inc.
Decision Date1986-09-24
Product CodeHAO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RAYLOR BONE IMPACTORS 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 1986-09-24 under 510(k) number K863415. The device is classified under product code HAO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAYLOR BONE IMPACTORS?

RAYLOR BONE IMPACTORS is a medical device that received FDA 510(k) clearance on 1986-09-24. The listed applicant is Cedar Surgical, Inc.. The 510(k) number is K863415.

When did RAYLOR BONE IMPACTORS receive FDA 510(k) clearance?

RAYLOR BONE IMPACTORS received FDA 510(k) clearance on 1986-09-24, under 510(k) number K863415.

Who is the listed applicant for RAYLOR BONE IMPACTORS?

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 BONE IMPACTORS?

The FDA product code for RAYLOR BONE IMPACTORS is HAO.

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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.

K873692RAYLOR(TM) DRILL STOPK872281RAYLOR FUSION FUNNELK873690CEDAR(TM) PELVIC CUSHIONK873691CEDAR(TM) RETRACTOR RINGK864425RAYLOR(TM) DISSECTING HOOKK864426RAYLOR(TM) DEPTH GAUGE

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Related Devices (Code: HAO)

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.

K220920Matreneu Percutaneous Balloon Compression KitShenzhen Shineyard Medical Device Co. , Ltd.K940973MULLAN GANGLION MICROCOMPRESSION SETCook, Inc.K951492RIB RESECTORUnited States Surgical, A Division of Tyco HealthcK943115AUTO SUTURE PITUITARY SPINAL RONGEURUnited States Surgical, A Division of Tyco HealthcK942968AUTO SUTURE SPINAL OSTEOTOMEUnited States Surgical, A Division of Tyco HealthcK942967AUTO SUTURE SPINAL CURETTEUnited States Surgical, A Division of Tyco Healthc

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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