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FDA 510(k)

COBB SPINAL ELEVATORS

K-Number: K882068 · 1988-06-03

ApplicantKarlin Technology, Inc.
Decision Date1988-06-03
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COBB SPINAL ELEVATORS is the device name listed in this FDA 510(k) record. The listed applicant is Karlin Technology, Inc.. It received FDA 510(k) clearance on 1988-06-03 under 510(k) number K882068. 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 COBB SPINAL ELEVATORS?

COBB SPINAL ELEVATORS is a medical device that received FDA 510(k) clearance on 1988-06-03. The listed applicant is Karlin Technology, Inc.. The 510(k) number is K882068.

When did COBB SPINAL ELEVATORS receive FDA 510(k) clearance?

COBB SPINAL ELEVATORS received FDA 510(k) clearance on 1988-06-03, under 510(k) number K882068.

Who is the listed applicant for COBB SPINAL ELEVATORS?

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

What is the FDA product code for COBB SPINAL ELEVATORS?

The FDA product code for COBB SPINAL ELEVATORS is KWP.

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Other records listing Karlin Technology, Inc. as applicant

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K903969SUCTION RETRACTOR(TOWER ATTACH.)FOR CRANK FRAM RETK893203BONE SCREWK893201BONE PLATEK882525SPINAL MICROKNIFEK882519X-RAY MARKERK882073SPINAL NEEDLE

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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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