The devices are intended to treat fractures of various bones, including the clavicle, scapyla, pelvis, long bone (humerus, ulna, radius, femur, tibia and fibula), and small bone (metacarpals, metatarsals, and phalanges) according to the standard of the AO Foundation (AO Principles of Fracture Management).

All app bone plates and screws are for single use only and are not intended for any spinal fixation procedures.

Device Description

The aap bone plate and screw implants are used for internal fixation of long and small bones. The plates are manufactured from commercial pure Titanium or Stainless Steel and the screws are manufactured from Titanium alloy or Stainless Steel.

AI/ML Overview

The provided text is a 510(k) summary for a medical device (aap Bone Plate and Screw Implants) and does not describe acceptance criteria for an AI/algorithm-based device, nor does it detail a study proving such a device meets acceptance criteria.

The document focuses on:

Identification of the device: Trade name, common name, classification, product code.
Submitter and Contact Information: Company details.
Performance Standards: References to cGMPs, ASTM requirements, and harmonized standards (ISO 13485:2003) for manufacturing and material specifications (Titanium, 316L Stainless Steel).
Intended Use: Description of fracture types and bones the implants are designed to treat, referencing AO Foundation principles.
Contraindications: Specific conditions where the device should not be used.
Device Description: Detailed list of various bone plates and screws with their dimensions and materials.
Predicate Devices: Comparison to other legally marketed bone plate and screw implants to establish substantial equivalence.
Sterilization Information: Instructions for end-user sterilization.
FDA Communication: Official letter from the FDA affirming the substantial equivalence and permitting marketing of the device.
Indications for Use Statement: Formal statement mirroring the intended use.

Therefore, I cannot extract the requested information regarding acceptance criteria, device performance tables, sample sizes for test/training sets, ground truth establishment, expert qualifications, adjudication methods, or MRMC/standalone studies, as this information is not present in the provided text. The document pertains to traditional medical device clearance based on substantial equivalence, not AI/algorithm performance.

Summary

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K072411

510(k) SUMMARY OF SAFETY AND EFFECTIVENESS

Submitters Name:	aap Implantate AGLorenzweg 512099 BerlinGermanyPhone: +49 30 750 19 0Fax: +49 30 750 19 111	MAR 20 2008
Contact Name:	Dipl.-Ing. Marc SeegersLorenzweg 512099 BerlinGermanyPhone: +49 30 750 19 192Fax: +49 30 750 19 111email: m.seegers@aap.de
Trade Name:	aap Bone Plate and Screw Implants
Common/Usual Name:	Bone fixation plate and screw
Classification Name:	Plate, Fixation, Bone Screw, Fixation, Bone
Device Class:	Class II
Product Code:	87 HRS87 HWC
Classification:	CFR Chapter I, Title 21 § 888.3030CFR Chapter I, Title 21 § 888.3040
Review Panel:	Orthopaedics

Performance Standards:

Devices are manufactured according to cGMP's, applicable ASTM require-. ments, and applicable harmonised standards ISO 13485:2003.
. The aap Bone plates are manufactured from commercial pure Titanium (cpTi ASTM F67 or ISO 5832-2) and 316L Stainless Steel (ASTM F139 or ISO 5832-1 ).
The agp Bone screws are manufactured from Titanium Alloy (ASTM F 136 or . ISO 5832-3) and (ASTM F 138 or ISO 5832-1).

Image /page/0/Picture/7 description: The image is a blurry, low-resolution photograph. Due to the poor quality, it is difficult to discern specific details or objects within the image. The overall impression is of an indistinct and unclear scene.

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2079111 캤시니

Intended Use:

The aap bone plates and screws are provided non-sterile in a tray or separately packed. The devices are intended to treat fractures of various bones, including the clavicle, scapula, pelvis, long bone (humerus, ulna, radius, femur, tibia and fibula), and small bone (metacarpals, metatarsals, and phalanges) according to the standard of the AO Foundation (AO Priciples of Fracture Management). All aap bone plates and screws are for single use only.

Contraindications

Inflammation, sepsis and osteomyelitis are absolute contraindications.

All applications that are not defined by the indications and the specialist literature are contraindicated.

All spinal fixation procedures.

In addition, surqical success can be adversely affected by:

acute or chronic infections, local or systemic �
vascular, muscular or neurological pathologies that compromise the � concerned extremity
all concomitant pathologies that could affect the function of the implant.
osteopathies with reduced bone substance such as severe osteoporosis ●
. Any mental or neuromuscular disorder that could result in an unacceptable risk of failure at the time of fixation or complications in post-operative treatment.
. Known or suspected sensitivity to metal
� Corpulence: an overweight or corpulent patient can strain the implant to such a degree that stabilization or implant failure can occur.
. Whenever the use of the implant comes into conflict with the anatomical structures of physiological status.

Other medical or surgical pre-conditions that could compromise the potentially beneficial procedure, such as:

the presence of tumors �
. congenital abnormalities
. immunosuppressive pathologies
increased sedimentation rates that cannot be explained by other pathologies
. increased leukocyte (WBC) count
. pronounced left shift in the differential leukocyte count.
Untreated malfunction of the metabolism .
Joint destruction caused by haemophilia, tabes or after infections �
Instability of the joint ligaments .

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Device Description: 得 - 在线 |

Plates (in brackets corresponding screw diameters):

. 4.5 ACP Broad Plate (ø6,5mm/ ø4.5mm)
4.5 ACP Narrow Plate (ø6,5mm/ ø4,5mm) .
Straight Reconstruction Plate 4.5 (ø4.5mm) .
T-Plate 4.5 (ø6,5mm/ ø4,5mm) ●
. T-Buttress Plate 4.5 (ø6,5mm/ ø4,5mm)
L-Buttress Plate 4.5 (ø6,5mm/ ø4,5mm) �
Spoon-Plate 4.5 (ø6,5mm/ ø4,5mm) .
3.5 ACP Straight Plate (ø4.0mm/ ø3.5mm) .
3.5 Straight Reconstruction Plate (ø3.5mm) ●
3.5 Cloverleaf Plate (ø4.0mm/ ø3.5mm) .
. 3.5 T-Plate (ø4.0mm/ ø3.5mm)
� 3.5 T-Plate olique angled (ø4.0mm/ ø3.5mm)
3.5 1/3 Tubular Plate (ø4.0mm/ ø3.5mm) .
2.7 Straight Plate (ø 2.7mm) .
2.7 Straight Reconstruction Plate (ø 2.7mm) .
2.7 Small T-Plate (ø 2.7mm) .
. 2.7 1/4 Tubular Plate (ø 2.7mm)
2.0 Straight Mini-Fragment Plate (ø2.0mm) .
Mini-Fragment T-Plate 2.0 (ø2.0mm) ●
. Mini-Fragment with straight L-Shape 2.0 (ø2.0mm)
. Mini-Fragment with oblique L-Shape 2.0 (ø2.0mm)

Screws:

ा में बाद में से मुक्त कर रहा है।
मुक्त कर रहा है कि कि में बाद में बाद में कि में बाद में कि में बाद में कि में कि में कि में कि में कि किसी की कहानी के लिए कहा कि कि में ब

Cortical Screw (ø1.5mm) .
Cortical Screw (ø2.0mm) and Cortical Screw selftapping (ø2.0mm) .
Cortical Screw (ø2.7mm) and Cortical Screw selftapping (ø2.7mm) ●
Cortical Screw (ø3.5mm) and Cortical Screw selftapping (ø3.5mm) .
Cortical Screw (ø4.5mm) and Cortical Screw selftapping (ø4.5mm) .
Cancellous Screw (ø4.0mm) and Cancellous Screw (ø4.0mm) with short . thread
. Cancellous Screw (ø6.5mm) with full thread
Cancellous Screw (ø6.5mm) with 16mm thread .
Cancellous Screw (ø6.5mm) with 32mm thread .

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KC73911 + 4

Predicate Devices for Substantial Equivalence:

The aap bone plates and screws are similar in size, material and intended use to
- Syntec-Taichung Bone Plate and Screw Implants (K983495) �
- Synthes Sterile 2.7mm Reconstruction Plates (K974908) .
- Synthes Bone Plates and Bone Screws for standard Osteosynthesis (Prea-. mendment
- Stryker Trauma Plating System (K000636) .
- Stryker Plating System Basic Fragment Set (K012162) .

Comparision of the technological Characteristics of the device to the predicate legally marketed devices:

There are no significant differences between the aap Bone Plate and Screw Implants and other systems currently being marketed which would adversely affect the use of the product. It is substantially equivalent to these other devices in design, function, materials and intended use.

Sterilisation Information:

؟ ﺍﻹ ﺍﻹﻃﺎﺭ

The devices are distributed in non sterile, recommendations for sterilization are contained in package insert. Note: These devices are sterilised by end users utilizing the approved/outlined guidelines found in the AAMI Guideline "Good Hospital Practice: Steam Sterilisation and Sterility Assurance" and in ANSI/AAMI/ISO 11737 quidelines to achieve the acceptable Sterility Assurance Level (SAL).

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DEPARTMENT OF HEALTH & HUMAN SERVICES

Image /page/4/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized eagle with its head turned to the left. The eagle's body is formed by three curved lines. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular pattern around the eagle.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

aap Implantate AG % Mr. Marc Seegers, Dipl .- Ing Director, QA/RA Lorenzweg 5 12099 Berlin Germany

Re: K072411 Trade/Device Name: aap Bone Plates and Screw Implants Regulation Number: 21 CFR 888.3030 Regulation Name: Single/multiple component metallic bone fixation appliances and accessories Regulatory Class: Class II Product Code: HRS, HWC Dated: March 14, 2008 Received: March 17, 2008

Dear Mr. Seegers:

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.

MAR 2 0 2008

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 - Mr. Marc Seegers, Dipl .- Ing.

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 Center for Devices and Radiological Health's (CDRH's) Office of Compliance at (240) 276-0120. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding postmarket surveillance, please contact CDRH's Office of Surveillance and Biometric's (OSB's) Division of Postmarket Surveillance at (240) 276-3474. For questions regarding the reporting of device adverse events (Medical Device Reporting (MDR)), please contact the Division of Surveillance Systems at (240) 276-3464. You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at toll-free number (800) 638-2041 or (240) 276-3150 or the Internet address http://www.fda.gov/cdrh/industry/support/index.html.

Sincerely yours.

Marti M. Millerson

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 Statement

Page 1 of 1

510(k) Number (if known): K072411

Device Name: aap Bone Plates and Screw Implants

Indications for Use:

All app bone plates and screws are for single use only and are not intended for any spinal fixation procedures.

Prescription Use X (Part 21 CFR 801 Subpart D)

(

AND/OR

Over-The-Counter Use (21 CFR 801 Subpart C)

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


	(Division Sign-Off)

Concurrence of CDRH, Office of Device Evaluation (ODE) Division of General, Restorative,and Neurological Devices

510(k) Number_K072411

Regulation Number and Section

§ 888.3030 Single/multiple component metallic bone fixation appliances and accessories.

(a)
Identification. Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.(b)
Classification. Class II.