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FDA 510(k)

CROSS ROUND & SQUARE SPINAL RODS & DIST. SPINAL

K-Number: K894472 · 1989-10-10

ApplicantBuckman Co., Inc.
Decision Date1989-10-10
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CROSS ROUND & SQUARE SPINAL RODS & DIST. SPINAL is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1989-10-10 under 510(k) number K894472. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CROSS ROUND & SQUARE SPINAL RODS & DIST. SPINAL?

CROSS ROUND & SQUARE SPINAL RODS & DIST. SPINAL is a medical device that received FDA 510(k) clearance on 1989-10-10. The listed applicant is Buckman Co., Inc.. The 510(k) number is K894472.

When did CROSS ROUND & SQUARE SPINAL RODS & DIST. SPINAL receive FDA 510(k) clearance?

CROSS ROUND & SQUARE SPINAL RODS & DIST. SPINAL received FDA 510(k) clearance on 1989-10-10, under 510(k) number K894472.

Who is the listed applicant for CROSS ROUND & SQUARE SPINAL RODS & DIST. SPINAL?

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

What is the FDA product code for CROSS ROUND & SQUARE SPINAL RODS & DIST. SPINAL?

The FDA product code for CROSS ROUND & SQUARE SPINAL RODS & DIST. SPINAL is KWP.

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Other records listing Buckman Co., 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.

K961320CROSS MEDICAL BONE PLATE SYSTEM/ CM BONE PLATE SYSTEM/CROSS TI BONE PLATE SYSTEMK974641FUTURELASE 3000/3002 ERBIUM LASER SYSTEMK964252ORTHOCHUCKK950099SYNERGY(TM) TI POSTERIOR SPINAL SYSTEMK960451WEBB-MORLEY SPINE SYSTEMK950999KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESIS

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Related Devices (Code: KWP)

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.

K133094CERTEX OCT SPINAL IMPLANT SYSTEMX-Spine Systems, Inc.K132504TIGER OCCIPITAL-CERVICAL-THORACIC SPINAL FIXATION SYSTEMCorelink, LLCK132900MARAUDER CERVICAL-THORACIC SPINAL FIXATION SYSTEMIntelligent Implant Systems, LLCK131427LOTUSSpinal Elements, Inc.K132332MOUNTAINEER OCT SPINAL SYSTEMMedos International SARLK131156LANX SPINAL FIXATION SYSTEMLanx, Inc.

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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