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FDA 510(k)

RANSFORD CERVICAL FIXATION SYSTEM

K-Number: K965221 · 1997-08-07

ApplicantSurgicraft , Ltd.
Decision Date1997-08-07
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RANSFORD CERVICAL FIXATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Surgicraft , Ltd.. It received FDA 510(k) clearance on 1997-08-07 under 510(k) number K965221. 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 RANSFORD CERVICAL FIXATION SYSTEM?

RANSFORD CERVICAL FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 1997-08-07. The listed applicant is Surgicraft , Ltd.. The 510(k) number is K965221.

When did RANSFORD CERVICAL FIXATION SYSTEM receive FDA 510(k) clearance?

RANSFORD CERVICAL FIXATION SYSTEM received FDA 510(k) clearance on 1997-08-07, under 510(k) number K965221.

Who is the listed applicant for RANSFORD CERVICAL FIXATION SYSTEM?

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

What is the FDA product code for RANSFORD CERVICAL FIXATION SYSTEM?

The FDA product code for RANSFORD CERVICAL FIXATION SYSTEM is KWP.

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Other records listing Surgicraft , Ltd. 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.

K091207SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICEK072370SURGICRAFT SURGICAL MESH SYSTEMK080447SURGICRAFT SCREW FIXATION SYSTEMK073109STALIF TT INTERVERTEBRAL BODY FUSION SYSTEMK072415STALIF (TM) CK051027STALIF TT

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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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