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FDA 510(k)

CEDAR(TM) PELVIC CUSHION

K-Number: K873690 · 1987-10-26

ApplicantCedar Surgical, Inc.
Decision Date1987-10-26
Product CodeLWG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CEDAR(TM) PELVIC CUSHION 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 1987-10-26 under 510(k) number K873690. The device is classified under product code LWG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEDAR(TM) PELVIC CUSHION?

CEDAR(TM) PELVIC CUSHION is a medical device that received FDA 510(k) clearance on 1987-10-26. The listed applicant is Cedar Surgical, Inc.. The 510(k) number is K873690.

When did CEDAR(TM) PELVIC CUSHION receive FDA 510(k) clearance?

CEDAR(TM) PELVIC CUSHION received FDA 510(k) clearance on 1987-10-26, under 510(k) number K873690.

Who is the listed applicant for CEDAR(TM) PELVIC CUSHION?

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 CEDAR(TM) PELVIC CUSHION?

The FDA product code for CEDAR(TM) PELVIC CUSHION is LWG.

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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 FUNNELK873691CEDAR(TM) RETRACTOR RINGK864425RAYLOR(TM) DISSECTING HOOKK864426RAYLOR(TM) DEPTH GAUGEK864421RAYLOR(TM) PERIOSTEAL ELEVATORS

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Related Devices (Code: LWG)

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.

K883295CHOP SPINE FRAMEAvec Scientific Design Corp.K882520SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADSKarlin Technology, Inc.K874494KAMBIN LAMINECTOMY FRAMEAvec Scientific Design Corp.

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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