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FDA 510(k)

LUMBAR IMPACTION SET

K-Number: K875290 · 1988-03-04

ApplicantT. Korossurgical Instruments Corp.
Decision Date1988-03-04
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LUMBAR IMPACTION SET is the device name listed in this FDA 510(k) record. The listed applicant is T. Korossurgical Instruments Corp.. It received FDA 510(k) clearance on 1988-03-04 under 510(k) number K875290. 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 LUMBAR IMPACTION SET?

LUMBAR IMPACTION SET is a medical device that received FDA 510(k) clearance on 1988-03-04. The listed applicant is T. Korossurgical Instruments Corp.. The 510(k) number is K875290.

When did LUMBAR IMPACTION SET receive FDA 510(k) clearance?

LUMBAR IMPACTION SET received FDA 510(k) clearance on 1988-03-04, under 510(k) number K875290.

Who is the listed applicant for LUMBAR IMPACTION SET?

The FDA 510(k) record lists T. Korossurgical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LUMBAR IMPACTION SET?

The FDA product code for LUMBAR IMPACTION SET is KWP.

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Other records listing T. Korossurgical Instruments Corp. 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.

K001915GRAFT MARKER RINGK002755NON-ABSORBING STERNATOMY MONOFILAMENT SUTUREK954016VIDEOSCOPE W/IRRIGATION SHEATHK953998DISCETOME TISSUE ASPIRATORK954052ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTESK954014PERCUTANEOUS DISCECTOMY CANNULA SYSTEM

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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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