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FDA 510(k)

SPINAL POSITIONING FRAME

K-Number: K922371 · 1992-06-04

ApplicantRhino Mfg.
Decision Date1992-06-04
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SPINAL POSITIONING FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Rhino Mfg.. It received FDA 510(k) clearance on 1992-06-04 under 510(k) number K922371. The device is classified under product code FQO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPINAL POSITIONING FRAME?

SPINAL POSITIONING FRAME is a medical device that received FDA 510(k) clearance on 1992-06-04. The listed applicant is Rhino Mfg.. The 510(k) number is K922371.

When did SPINAL POSITIONING FRAME receive FDA 510(k) clearance?

SPINAL POSITIONING FRAME received FDA 510(k) clearance on 1992-06-04, under 510(k) number K922371.

Who is the listed applicant for SPINAL POSITIONING FRAME?

The FDA 510(k) record lists Rhino Mfg. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPINAL POSITIONING FRAME?

The FDA product code for SPINAL POSITIONING FRAME is FQO.

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.

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Other records listing Rhino Mfg. 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.

K924700FISK HEADREST

Related Devices (Code: FQO)

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.

K240598Maestro System (REF100)Moon SurgicalK221410Maestro PlatformMoon SurgicalK090136STERIS CMAX XLT SURGICAL TABLESTERIS CorporationK972810OPT80 THE TRANSPORTABLE (OPT80)O.P.T. USA, Inc.K971988ALLEN, ULTRA AND SMART SOCKETSAllen Medical Systems, Inc.K971307AMSCO SURGICAL TABLESTERIS Corporation

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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