The KLS Martin Quick Disc is intended for use in the reattachment of cranial bone flaps after a craniotomy, covering burr holes, and fixation of cranial fractures.

Device Description

The KLS Martin Quick Disc is a two-sided cranial closure device. The lower disc is attached to a threaded post. The upper disc is threaded down and locked on the post securely holding the bone flap in place. The KLS Martin Quick Disc diameters range from 12mm to 22mm in size

AI/ML Overview

The provided text is a 510(k) summary for the KLS Martin Quick Disc, a cranial closure device. It describes the device, its intended use, and its substantial equivalence to predicate devices. However, this document does not contain any information about acceptance criteria, clinical studies, sample sizes, ground truth establishment, or expert involvement as requested in the prompt for evaluating device performance.

Therefore, I cannot provide the requested table and detailed study information because the source document does not contain this data. The 510(k) summary is focused on establishing substantial equivalence based on intended use, material composition, and principle of operation, rather than presenting performance data from specific studies with acceptance criteria.

Summary

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kls martin L.P.

KO62857

510(K) SUMMARY

NOV 2 2 2006

Submitter:	KLS-Martin, L.P.11239-1 St. Johns Industrial Parkway SouthJacksonville, FL 32246Phone: 904-641-7746Fax: 904-641-7378
Contact Person:	Jennifer DamatoDirector RA/QA
Date of Summary:	9 September 2006
Device Name:	KLS Martin Quick Disc
Trade Name:	Quick Disc
Common Name:	Plate, Cranioplasty
ClassificationName and Number:	Preformed Nonalterable Cranioplasty Plate(CFR 882.5330)
Regulatory Class:	II
Predicate Devices:	CranioFix Titanium Clamp System (K040864)Spin Down RapidFlap (K031034)OsteoMed Cranial Flap Fixation System (K022277)Synthes Cranial Flap Twist Clamp (K991860)Aesculap CranioFix Titanium Clamp System (K972332)
Intended Use:	The KLS Martin Quick Disc is intended for usein the reattachment of cranial bone flaps after acraniotomy, covering burr holes, and fixation ofcranial fractures.

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Device Description:

Technological Characteristics:

Similarities to Predicate

The KLS Martin Quick Disc is similar in intended use, material composition and principle as the CranioFix Titanium Clamp System (K040864), Spin Down RapidFlap (K031034), OsteoMed Cranial Flap Fixation System (K022277), Synthes Cranial Flap Twist Clamp (K991860), and Aesculap CranioFix Titanium Clamp System (K972332). The KLS Martin Quick Disc is similar in fixation as the Aesculap CranioFix Titanium Clamp System (K972332)

Substantial Equivalence:

The KLS Martin Quick Disc is substantially equivalent in intended use, material composition and principle to the CranioFix Titanium Clamp System (K040864), Spin Down RapidFlap (K031034), OsteoMed Cranial Flap Fixation System (K022277), Synthes Cranial Flap Twist Clamp (K991860), and Aesculap CranioFix Titanium Clamp System (K972332).

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Image /page/2/Picture/1 description: The image shows the seal of the U.S. Department of Health & Human Services. The seal is circular and contains the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. In the center of the seal is an abstract image of an eagle.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

KLS Martin, L.P % Ms. Jennifer Damato 11239 St. Johns Industrial Parkway South Jacksonville, Florida 32246

NOV 2 2 2006

Re: K062857

Trade/Device Name: KLS Martin Quick Disc Regulation Number: 21 CFR 882.5330 Regulation Name: Preformed nonalterable cranioplasty plate Regulatory Class: Class II Product Code: GXN Dated: September 9, 2006 Received: September 25, 2006

Dear Ms. Damato:

We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food. Drug. and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations. Title 21, Parts 800 to 898. In addition. FDA may publish further announcements concerning your device in the Federal Register.

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

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Page 2 - Ms. Jennifer Damato

This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (240) 276-0210 Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.

Sincerely vours

Barbara Buelow

Mark N. Melkerson Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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Indications for Use

510(k) Number (if known):

Device Name: KLS Martin Quick Disc

Indications For Use:

The KLS Martin Quick Disc is intended for use in the reattachment of cranial bone flaps after a craniotomy, covering burr holes, and fixation of cranial fractures.

Prescription Use V (Part 21 CFR 801 Subpart D)

AND/OR

Over-The-Counter Use (21 CFR 807 Subpart C)

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

Darbar Buelm

(Division Sign-Off) Division of General, Restorative, and Nearological Devices

510(k) Number K062857

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Regulation Number and Section

§ 882.5330 Preformed nonalterable cranioplasty plate.

(a)
Identification. A preformed nonalterable cranioplasty plate is a device that is implanted in a patient to repair a skull defect and is constructed of a material, e.g., stainless steel or vitallium, that cannot be altered or reshaped at the time of surgery without changing the chemical behavior of the material.(b)
Classification. Class II (performance standards).