3.Omm Biomet Cannulated Screw System

K143188 · Biomet Manufacturing Corp · HWC · Dec 30, 2014 · Orthopedic

Device Facts

• Record ID: K143188
• Device Name: 3.Omm Biomet Cannulated Screw System
• Applicant: Biomet Manufacturing Corp
• Product Code: HWC · Orthopedic
• Decision Date: Dec 30, 2014
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 888.3040
• Device Class: Class 2
• Attributes: Therapeutic

Intended Use

1. Fixation of small bones, including those in the foot, patella, ankle, wrist and elbow. 2. Arthrodesis of the foot, wrist and elbow. 3. Small and long bone osteotomies. 4. Fracture fixation of small bones, small bone fragments and long bones.

Device Story

System consists of Ti-6Al-4V alloy partially threaded bone screws and washers; includes dimensionally optimized instruments. Used by orthopedic surgeons in clinical settings to stabilize fractures, perform osteotomies, or achieve arthrodesis. Screws are implanted to provide mechanical fixation of bone fragments; instruments aid in alignment and stabilization. Benefits include skeletal stabilization and fracture healing support. Offered in sterile and non-sterile configurations.

Clinical Evidence

No clinical data provided. Substantial equivalence is supported by non-clinical bench testing, including torsional, axial pullout, and insertion/removal torque tests per ASTM F543, and engineering analysis comparing torsional yield strengths to predicate devices.

Technological Characteristics

Materials: Ti-6Al-4V alloy per ASTM F136. Design: Partially threaded cannulated screws with washers. Mechanical testing: ASTM F543 (torsional, axial pullout, insertion/removal torque). Sterilization: Identical to K140891. Connectivity: None (mechanical device).

Indications for Use

Indicated for fixation of small bones (foot, patella, ankle, wrist, elbow), arthrodesis of foot/wrist/elbow, small and long bone osteotomies, and fracture fixation of small bones, small bone fragments, and long bones.

Regulatory Classification

Identification

A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.

Predicate Devices

• Biomet Cannulated Screw System (K140891)
• BioDrive Cannulated Screw System (K082874)
• Synthes Sterile 3.0 mm Cannulated Screw and Threaded Washer (K962823)
• FRS Screw (K062352)
• Wright Compression Screws (DartFire) (K082320)

Submission Summary (Full Text)

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Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002

Biomet Manufacturing Corporation Ms. Suzana Otaño Regulatory Affair Manager 56 East Bell Drive PO Box 587 Warsaw, Indiana 46581

December 30, 2014

Re: K143188

Trade/Device Name: 3.0mm Biomet Cannulated Screw System Regulation Number: 21 CFR 888.3040 Regulation Name: Smooth or threaded metallic bone fixation fastener Regulatory Class: Class II Product Code: HWC Dated: November 3, 2014 Received: November 5, 2014

Dear Ms. Otaño:

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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you; however, that device labeling must be truthful and not misleading.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to 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); medical device reporting (reporting of medical

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Page 2 - Ms. Suzana Otaño

device-related adverse events) (21 CFR 803); 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.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to

http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.

Sincerely yours.

# Mark N. Melkerson -S

Mark N. Melkerson Director Division of Orthopedic Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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# Indications for Use

510(k) Number (if known)

#### K143188

Device Name

3.0mm Biomet Cannulated Screw System

Indications for Use (Describe)

- 1. Fixation of small bones, including those in the foot, patella, ankle, wrist and elbow.
- 2. Arthrodesis of the foot, wrist and elbow.
- 3. Small and long bone osteotomies.

4. Fracture fixation of small bones, small bone fragments and long bones.

Type of Use (Select one or both, as applicable)

| <div> <span style="font-size: 16px;">☑</span> Prescription Use (Part 21 CFR 801 Subpart D) </div> |
|---------------------------------------------------------------------------------------------------------------|
| <div> <span style="font-size: 16px;">☐</span> Over-The-Counter Use (21 CFR 801 Subpart C) </div> |

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# 510(k) Summary

In accordance with 21 CFR §807.92 and the Safe Medical Devices Act of 1990, the following information is provided for the 3.0mm Biomet Cannulated Screw System 510(k) premarket notification.

| Sponsor: | Biomet Manufacturing Corp.<br>56 East Bell Drive<br>PO Box 587<br>Warsaw, IN 46581<br>Establishment Registration Number: 1825034 |
|-----------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Contact: | Suzana Otaño<br>Regulatory Affairs Manager, Trauma<br>Phone: [phone] |
| Date: | December 19, 2014 |
| Subject Device: | Trade Name: 3.0mm Biomet Cannulated Screw System<br>Common Name: Screw, Fixation, Bone<br>Classification Name:<br>• HWC- Smooth or Threaded Metallic Bone Fixation Fastener (21 CFR 888.3040) |

#### Legally marketed devices to which substantial equivalence is claimed:

- Biomet Cannulated Screw System - K140891
- BioDrive Cannulated Screw System - K082874
- Synthes Sterile 3.0 mm Cannulated Screw and Threaded Washer - K962823
- FRS Screw K062352 ●
- Wright Compression Screws (DartFire) – K082320

#### Device Description

The 3.0mm Biomet Cannulated Screw System consists of bone screws of various lengths and are Ti alloy partially threaded screws with the associated 3.0mm washer. They are offered in both a sterile and non-sterile configuration. The 3.0mm Biomet Cannulated Screw System also contains dimensionally optimized corresponding instruments which are used with the 3.0mm Biomet Cannulated Screws and washers to aid in the alignment and stabilization of fractures to the skeletal system.

#### Intended Use and Indications for Use

- 1. Fixation of small bones, including those in the foot, patella, ankle, wrist and elbow.
- 2. Arthrodesis of the foot, wrist and elbow.
- 3. Small and long bone osteotomies.
- 4. Fracture fixation of small bones, small bone fragments and long bones.

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## Summary of Technological Characteristics

The rationale for substantial equivalence is based on consideration of the following technological characteristics:

- Materials: The Biomet Cannulated Screw System screws and washers are fabricated from Ti-6Al-4V alloy per ASTM F136. The materials used in the 3.0mm Biomet Cannulated Screw System are identical to those used in K140891, and similar to those used in K082874, and K962823.
- Design Features: The 3.0mm Biomet Cannulated Screws are similar in design and dimension to the Biomet Cannulated Screw System cleared via K140891 and are considered a line extension. The design of the subject device is similar to those cleared in K082874 and K962823.
- . Sterilization: The sterilization configurations of the 3.0mm Biomet Cannulated Screw System is identical to that of the Biomet Cannulated Screw System cleared via K140891. The sterilization configurations are similar to that of the devices cleared via K082874 and K962823.

## Summary of Performance Data (Nonclinical and/or Clinical)

- . Non-Clinical Tests
- Non-clinical performance testing included torsional, axial pullout and o insertion/removal torque mechanical tests per ASTM F543. The axial pullout and insertion/removal torque values were equal to or better than the predicate devices. Engineering analysis of the torsional yield strengths demonstrated that the 3.0mm Biomet Cannulated Screws have equal to or better torsional yield strength than the predicate screws including the FRS screw (K062352) and the DartFire screw (K082320). Results of bench testing in conjunction with engineering analysis indicate that the subject screws are substantially equivalent to legally marketed devices offering a reasonable assurance of safety and effectiveness.
- Clinical Tests
- None provided as a basis for substantial equivalence. o

## Substantial Equivalence Conclusion

The 3.0mm Biomet Cannulated Screw System is substantially equivalent to the commercially available Biomet Cannulated Screw System cleared via K140891, as well as the devices cleared via K082874, K082320, K062352 and K962823.