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FDA 510(k)

NEUROSURGICAL HEADREST

K-Number: K853799 · 1985-10-07

ApplicantCedar Surgical, Inc.
Decision Date1985-10-07
Product Code
DecisionSubstantially Equivalent

Device Summary

NEUROSURGICAL HEADREST 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 1985-10-07 under 510(k) number K853799. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROSURGICAL HEADREST?

NEUROSURGICAL HEADREST is a medical device that received FDA 510(k) clearance on 1985-10-07. The listed applicant is Cedar Surgical, Inc.. The 510(k) number is K853799.

When did NEUROSURGICAL HEADREST receive FDA 510(k) clearance?

NEUROSURGICAL HEADREST received FDA 510(k) clearance on 1985-10-07, under 510(k) number K853799.

Who is the listed applicant for NEUROSURGICAL HEADREST?

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

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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 HOOKK864421RAYLOR(TM) PERIOSTEAL ELEVATORS

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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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