K Number
K072562
Device Name
MICROWARE BONE PLATES AND BONE SCREWS
Date Cleared
2008-12-04

(450 days)

Product Code
Regulation Number
888.3030
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Microware Bone Plates and Bone Screws are provided non-sterile. Microware Bone Plates and Bone Screws are intended to treat fractures of various bones, including the clavicle, pelvis, scapula, long bone (humerus, ulna, radius, femur, tibia and fibula), and small bone (metacarpals, metatarsals and phalanges). Microware DHS/DCS Plate System is provided non-sterile. Microware DHS/DCS Plate System is intended for use in fixation of fractures to the proximal femur. The system is indicated for use in trochanteric, pertrochanteric, intertrochanteric, and basilar neck fracture.
Device Description
The Bone Plates and Bone Screws system & DHS/DCS Plate System consist of non-sterile bone plate and bone screw implants. The plates are devices, which are fastened to bone for purpose of providing fixation. They are principally differentiated by their function. Thus there are five kinds of styles: dynamic compression plate (DCP), tubular, special, mini and dynamic hip screw/dynamic condylar screw (DHS/DCS). The shape of the plate is an adaptation of the plate to the local anatomy and doesn't denote any function. Thus the name depends on the biomechanical function the plate is performing. Every plate is divided various types as following: Plate Name | Geometry Shane ---|--- 3 | lengthening-narrow, broad, lengthening-broad, straight Special | L-shaped, T-shaped, spoon, cobra, lateral tibia head, condylar buttress, head, and hook Mini | Straight, L-shaped, T-shaped, condylar, special, and reconstruction DHS/DCS | Dynamic Hip Screw, Dynamic Condylar Screw The series in size of Microware bone screws and bone plates except DHS/DCS are divided into mini, small and large. The range of plates in thickness are from 1.0 to 6.0 mm, width from 3.8 to 17 mm, length from 17 to 359 mm, and hole number from 2 to 22 holes. On the other hand, the screws used either to fasten plates or similar devices onto bone, or, as lag screws, to hold together fragments of bone. The screws are differentiated by the manner in which they are inserted into bone, their function, their size, and the type of bone they are intended for. Thus there are four kinds of style: cortex, cancellous, malleolar, and cannulated. All screws have a hexagonal recess; this feature has proven itself to be of great advantage at the time of the screw removal and insertion. The range of screws in thread is diameter from 1.5 to 7.3 mm, total length from 6 to 150 mm. The DHS/DCS Plate System consists of DHS/DCS plate, DHS/DCS Screw, DHS/DCS Compression Screw, and 4.5mm Cortex Screw (self-tapping). The DHS Plates are available with short and standard barrel which length is 25mm and 38mm respectively. And the barrel angles are available in 95', 135 , 140', 145', and 150'. The self-tapping 4.5mm Cortex Serew can be used to fix the DHS/DCS Plate to the femoral shaft. The DHS/DCS Screw is available in total length from 50 to 145mm, thread length 22mm, shaft diameter 7.9mm, and outer diameter 12.5 to 14mm. The thread of DHS/DCS screw has a buttress type. The DHS/DCS Compression Screw can be used to achieve fracture compression. Its dimension is available with thread length 26mm and outer diameter 4.0mm.
More Information

Not Found

No
The device description focuses solely on the physical characteristics and intended use of bone plates and screws, with no mention of software, algorithms, or data processing that would indicate AI/ML.

Yes.

The device is intended to treat fractures of various bones, which is a therapeutic purpose.

No

The device is composed of bone plates and screws intended for the fixation of bone fractures. It doesn't analyze, measure, or process clinical data to provide diagnostic information.

No

The device description clearly outlines physical bone plates and screws made of materials like metal, which are hardware components. There is no mention of any software functionality.

No, this device is not an IVD (In Vitro Diagnostic).

Here's why:

  • IVD Definition: In Vitro Diagnostic devices are used to examine specimens taken from the human body (like blood, urine, tissue) to provide information about a person's health. This testing is done outside of the body (in vitro).
  • Device Description: The provided text describes bone plates and screws that are surgically implanted into the body to fix fractures. This is a therapeutic device used within the body (in vivo).
  • Intended Use: The intended use is to "treat fractures of various bones" and "fixation of fractures." This is a direct treatment of a physical condition, not a diagnostic test performed on a specimen.

The device described is a surgical implant used for orthopedic fixation.

N/A

Intended Use / Indications for Use

Microware Bone Plates and Bone Screws are provided non-sterile. Microware Bone Plates and Bone Screws are intended to treat fractures of various bones, including the clavicle, pelvis, scapula, long bone (humerus, ulna, radius, femur, tibia and fibula), and small bone (metacarpals, metatarsals and phalanges).

Microware DHS/DCS Plate System is provided non-sterile. Microware DHS/DCS Plate System is intended for use in fixation of fractures to the proximal femur. The system is indicated for use in trochanteric, pertrochanteric, and basilar neck fracture.

Product codes (comma separated list FDA assigned to the subject device)

HRS, HWC, KTT

Device Description

The Bone Plates and Bone Screws system & DHS/DCS Plate System consist of non-sterile bone plate and bone screw implants. The plates are devices, which are fastened to bone for purpose of providing fixation. They are principally differentiated by their function. Thus there are five kinds of styles: dynamic compression plate (DCP), tubular, special, mini and dynamic hip screw/dynamic condylar screw (DHS/DCS). The shape of the plate is an adaptation of the plate to the local anatomy and doesn't denote any function. Thus the name depends on the biomechanical function the plate is performing. Every plate is divided various types as following:

Plate NameGeometry Shane
Dynamic Compression Plate (DCP)lengthening-narrow, broad, lengthening-broad, straight
Tubularone-third
SpecialL-shaped, T-shaped, spoon, cobra, lateral tibia head, condylar buttress, head, and hook
MiniStraight, L-shaped, T-shaped, condylar, special, and reconstruction
DHS/DCSDynamic Hip Screw, Dynamic Condylar Screw

The series in size of Microware bone screws and bone plates except DHS/DCS are divided into mini, small and large. The range of plates in thickness are from 1.0 to 6.0 mm, width from 3.8 to 17 mm, length from 17 to 359 mm, and hole number from 2 to 22 holes.

On the other hand, the screws used either to fasten plates or similar devices onto bone, or, as lag screws, to hold together fragments of bone. The screws are differentiated by the manner in which they are inserted into bone, their function, their size, and the type of bone they are intended for. Thus there are four kinds of style: cortex, cancellous, malleolar, and cannulated. All screws have a hexagonal recess; this feature has proven itself to be of great advantage at the time of the screw removal and insertion. The range of screws in thread is diameter from 1.5 to 7.3 mm, total length from 6 to 150 mm.

The DHS/DCS Plate System consists of DHS/DCS plate, DHS/DCS Screw, DHS/DCS Compression Screw, and 4.5mm Cortex Screw (self-tapping). The DHS Plates are available with short and standard barrel which length is 25mm and 38mm respectively. And the barrel angles are available in 95', 135 , 140', 145', and 150'. The self-tapping 4.5mm Cortex Serew can be used to fix the DHS/DCS Plate to the femoral shaft.

The DHS/DCS Screw is available in total length from 50 to 145mm, thread length 22mm, shaft diameter 7.9mm, and outer diameter 12.5 to 14mm. The thread of DHS/DCS screw has a buttress type.

The DHS/DCS Compression Screw can be used to achieve fracture compression. Its dimension is available with thread length 26mm and outer diameter 4.0mm.

Mentions image processing

Not Found

Mentions AI, DNN, or ML

Not Found

Input Imaging Modality

Not Found

Anatomical Site

clavicle, pelvis, scapula, long bone (humerus, ulna, radius, femur, tibia and fibula), small bone (metacarpals, metatarsals and phalanges), proximal femur (trochanteric, pertrochanteric, intertrochanteric, and basilar neck fracture)

Indicated Patient Age Range

Not Found

Intended User / Care Setting

Not Found

Description of the training set, sample size, data source, and annotation protocol

Not Found

Description of the test set, sample size, data source, and annotation protocol

Not Found

Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)

Not Found

Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)

Not Found

Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.

K983495, K983873, K063020

Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.

Not Found

Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).

Not Found

§ 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.

0

3. 510(k) Summary of Safety and Effectiveness

Submitter's Name: Microware Precision Co., Ltd.

DEC 0 4 2008

Address: No. 12, Keyuan 2nd Rd., Situn District, Taichung City 40763, Taiwan Phone No: +886-4-24636275 Fax No: +886-4-24636276

Contact Person: Harrison Du

Preparation date: April 7, 2008

Registration Number:

Device Name: Microware Bone Plates and Bone Screws & Microware DHS/DCS Plate System

Proprietary Name: Microware Bone Plates and Bone Screws & Microware DHS/DCS Plate System

Common Name: Bone Fixation Plate and Screw

Classification Name

Classification Name: Class II: Plate, Fixation, Bone HRS-CFR 888.3030 Class II: Screw, Fixation, Bone HWC-CFR 888.3040 Class II: Appliance, fixation, nail/blade/plate Combination, multiple component KTT-CFR 888.3030

Product Code: HRS, HWC, KTT

Panel Code: Orthopedic/87

Microware Precision Co., Ltd.

510(k) submission 2008

1

K072562 (pg. 2 of

Predicate Device Information:

Syntec-Taichung Non-sterile Bone Plate and Screw Implants (K983495) Syntec-Taichung Non-sterile DHS/DCS Plate System (K983873) INTAI Bone Plate and Bone Screw System & INTAI DHS/DCS Plate System (K063020)

Materials:

The non-sterile bone plates and screws are manufactured from commercial medical use 316L stainless steel that meet ASTM F138 and ASTM F139, and titanium alloy (Ti-6Al-4V) that meet ASTM F136.

Indication for use:

Microware Bone Plates and Bone Screws are provided non-sterile. Microware Bone Plates and Bone Screws are intended to treat fractures of various bones, including the clavicle, pelvis, scapula, long bone (humerus, ulna, radius, femur, tibia and fibula), and small bone (metacarpals, metatarsals and phalanges).

Microware DHS/DCS Plate System is provided non-sterile. Microware DHS/DCS Plate System is intended for use in fixation of fractures to the proximal femur. The system is indicated for use in trochanteric, pertrochanteric, and basilar neck fracture.

Device Description:

The Bone Plates and Bone Screws system & DHS/DCS Plate System consist of non-sterile bone plate and bone screw implants. The plates are devices, which are fastened to bone for purpose of providing fixation. They are principally differentiated by their function. Thus there are five kinds of styles: dynamic compression plate (DCP), tubular, special, mini and dynamic hip screw/dynamic condylar screw (DHS/DCS). The shape of the plate is an adaptation of the plate to the local anatomy and doesn't denote any function. Thus the name depends on the biomechanical function the plate is performing. Every plate is divided various types as following:

| State for Children Call College College Company College Come Call - Callery
Plate Name
| Geometry Shane |
|-----------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| 3 | Canada A. callery and contractive de la proposed and consideration of the complex of the complex of the complex of the consisted to the consisted to the consideration of the
Charles Collection Control And
.

lengthening-narrow, broad, lengthening-broad, straight |
| |

one-third.
יצורים חיצוניים

ARTI

Microware Precision Co., Ltd.

2

KOT2562 (Pg. 30f4)

| Special | L-shaped, T-shaped, spoon, cobra, lateral tibia head, condylar
buttress, head, and hook |
|---------|--------------------------------------------------------------------------------------------|
| Mini | Straight, L-shaped, T-shaped, condylar, special, and
reconstruction |
| DHS/DCS | Dynamic Hip Screw, Dynamic Condylar Screw |

The series in size of Microware bone screws and bone plates except DHS/DCS are divided into mini, small and large. The range of plates in thickness are from 1.0 to 6.0 mm, width from 3.8 to 17 mm, length from 17 to 359 mm, and hole number from 2 to 22 holes.

On the other hand, the screws used either to fasten plates or similar devices onto bone, or, as lag screws, to hold together fragments of bone. The screws are differentiated by the manner in which they are inserted into bone, their function, their size, and the type of bone they are intended for. Thus there are four kinds of style: cortex, cancellous, malleolar, and cannulated. All screws have a hexagonal recess; this feature has proven itself to be of great advantage at the time of the screw removal and insertion. The range of screws in thread is diameter from 1.5 to 7.3 mm, total length from 6 to 150 mm.

The DHS/DCS Plate System consists of DHS/DCS plate, DHS/DCS Screw, DHS/DCS Compression Screw, and 4.5mm Cortex Screw (self-tapping). The DHS Plates are available with short and standard barrel which length is 25mm and 38mm respectively. And the barrel angles are available in 95', 135 , 140', 145', and 150'. The self-tapping 4.5mm Cortex Serew can be used to fix the DHS/DCS Plate to the femoral shaft.

The DHS/DCS Screw is available in total length from 50 to 145mm, thread length 22mm, shaft diameter 7.9mm, and outer diameter 12.5 to 14mm. The thread of DHS/DCS screw has a buttress type.

The DHS/DCS Compression Screw can be used to achieve fracture compression. Its dimension is available with thread length 26mm and outer diameter 4.0mm.

Substantial Equivalence:

A comparison between the proposed device and the predicate device has shown that three devices are very similar or identical in terms of indication for use, material, followed performance and standard and sterilization, and no significant difference between the proposed and predicate devices has been found. Thus, the "Microware Bone Plates and Bone Screws &

Microware Precision Co., Ltd

510(k) submission 200

3

Microware DHS/DCS Plate System" is substantially equivalent to Syntec-Taichung Non-sterile Bone Plate and Screw implants (K983495), Syntec-Taichung Non-sterile DHS/DCS Plate System (K983873), and INTAI Bone Plate and Bone Screw System & INTAI DHS/DCS Plate System (K063020).

Microware Precision Co., Ltd.

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

510(k) submission 2008

4

DEPARTMENT OF HEALTH & HUMAN SERVICES

Image /page/4/Picture/1 description: The image shows the seal of the U.S. Department of Health and Human Services. The seal features an eagle-like symbol in the center, with its wings forming three curved lines. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular pattern around the eagle. The text is in all capital letters and is evenly spaced around the circle.

Public Health Service

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

Microware Precision Co., Ltd. c/o Mr. Harrison Du General Manager No. 12. Keyuan 2nd Rd. Situn District Taichung City 40763, TAIWAN

DEC 0 4 2008

Re: K072562

Trade/Device Name: Microware Bone Plates and Bone Screws & Microware DHS/DCS Plate System

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, KTT Dated: October 22, 2008

Received: November 3, 2008

Dear Mr. Du:

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

5

Page 2 - Mr. Harrison Du

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 (OS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. 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 Biometrics' (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 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 yours,

Mark N. Millenson

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

Enclosure

6

Indications for Use 2.

510(k) Number (if known): Ko 72562

Device Name: Microware Bone Plates and Bone Screws Indications for Use:

Microware Bone Plates and Bone Screws are provided non-sterile. Microware Bone Plates and Bone Screws are intended to treat fractures of various bones, including the clavicle, pelvis, scapula, long bone (humerus, ulna, radius, femur, tibia and fibula), and small bone (metacarpals, metatarsals and phalanges).

Microware DHS/DCS Plate System is provided non-sterile. Microware DHS/DCS Plate System is intended for use in fixation of fractures to the proximal femur. The system is indicated for use in trochanteric, pertrochanteric, intertrochanteric, and basilar neck fracture.

Prescription Use (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 IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

(Division Sign-Off)

Division of General, Restorative and Neurological Devices

510(k) Number
-----------------

(Division Sign-Off)

Division of General, Restorative,

and Neurological Devices

510(k) NumberK072562
------------------------

510(k) submission 2008

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