Mini Superhawk Suture Anchor System

K253010 · Responsive Arthroscopy, LLC · MBI · Oct 14, 2025 · Orthopedic

Device Facts

• Record ID: K253010
• Device Name: Mini Superhawk Suture Anchor System
• Applicant: Responsive Arthroscopy, LLC
• Product Code: MBI · Orthopedic
• Decision Date: Oct 14, 2025
• Decision: SESE
• Submission Type: Special
• Regulation: 21 CFR 888.3040
• Device Class: Class 2
• Attributes: Therapeutic

Intended Use

The Mini Superhawk Suture Anchors are intended to be used for fixation of suture (soft tissue) to bone in the shoulder, foot/ankle, hip, knee, hand/wrist, and elbow in the following procedures: - Shoulder: Rotator Cuff Repair, Bankart Repair, SLAP Lesion Repair, Biceps Tenodesis, Acromio-Clavicular Separation Repair, Deltoid Repair, Capsular Shift or Capsulolabral Reconstruction. - Foot/Ankle: Lateral Stabilization, Medial Stabilization, Achilles Tendon Repair, Hallux Valgus Reconstruction, Mid-foot Reconstruction, Metatarsal Ligament Repair/Tendon Repair, Bunionectomy, Digital Tendon Transfers. - Knee: Medial Collateral Ligament Repair, Lateral Collateral Ligament Repair, Vastus Medialis Obliquus Advancement, Patellar Tendon Repair, Posterior Oblique Ligament Repair, Iliotibial Band Tenodesis, Joint Capsule Closure. - Hand/Wrist: Scapholunate Ligament Reconstruction, Ulnar or Radial Collateral Ligament Reconstruction. - Elbow: Biceps Tendon Reattachment, Tennis Elbow Repair, Ulnar or Radial Collateral Ligament Reconstruction, Lateral Epicondylitis Repair. - Hip: Capsular Repair, Acetabular Labral Repair.

Device Story

System comprises PEEK suture anchors for soft tissue-to-bone fixation; includes 3.75mm screw-in anchor with 1.5mm suture tape and 3.75mm knotless push-in anchor. Anchors preloaded on inserters; provided sterile via ethylene oxide. Used by surgeons in clinical settings for various orthopedic repairs (e.g., rotator cuff, ligament reconstruction). Device functions by anchoring suture into bone to secure soft tissue; screw-in mechanism provides mechanical fixation, while push-in anchor utilizes knotless locking. Output is physical fixation of tissue; assists surgeon in restoring anatomical integrity. Benefits include secure tissue attachment and procedural efficiency.

Clinical Evidence

Bench testing only. Testing included insertion torque, insertion force, suture locking force, and cyclic pullout force. All results met acceptance criteria and demonstrated performance equivalent to predicate devices.

Technological Characteristics

Material: PEEK; Principle: Mechanical bone fixation (screw-in/push-in); Form factor: 3.75mm diameter anchors; Sterilization: Ethylene oxide (EO); Single-use; Pre-loaded on inserters.

Indications for Use

Indicated for soft tissue-to-bone fixation in shoulder, foot/ankle, hip, knee, hand/wrist, and elbow orthopedic procedures.

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

• Responsive Arthroscopy Knotless Push-in Suture Anchor System (K202153)
• Responsive Arthroscopy Mustang Suture Anchors (K222763)

Submission Summary (Full Text)

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FDA U.S. FOOD & DRUG ADMINISTRATION

October 14, 2025

Responsive Arthroscopy, LLC
Gretchen Hinchley
VP of Quality, Regulatory, and Compliance
701 N. 3rd Street
Suite 208
Minneapolis, Minnesota 55401

Re: K253010
Trade/Device Name: Mini Superhawk Suture Anchor System
Regulation Number: 21 CFR 888.3040
Regulation Name: Smooth or threaded metallic bone fixation fastener
Regulatory Class: Class II
Product Code: MBI
Dated: September 16, 2025
Received: September 19, 2025

Dear Gretchen Hinchley:

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 (the 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. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database available at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. 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.

U.S. Food & Drug Administration
10903 New Hampshire Avenue
Silver Spring, MD 20993
www.fda.gov

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K253010 - Gretchen Hinchley
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Additional information about changes that may require a new premarket notification are provided in the FDA guidance documents entitled "Deciding When to Submit a 510(k) for a Change to an Existing Device" (https://www.fda.gov/media/99812/download) and "Deciding When to Submit a 510(k) for a Software Change to an Existing Device" (https://www.fda.gov/media/99785/download).

Your device is also subject to, among other requirements, the Quality System (QS) regulation (21 CFR Part 820), which includes, but is not limited to, 21 CFR 820.30, Design controls; 21 CFR 820.90, Nonconforming product; and 21 CFR 820.100, Corrective and preventive action. Please note that regardless of whether a change requires premarket review, the QS regulation requires device manufacturers to review and approve changes to device design and production (21 CFR 820.30 and 21 CFR 820.70) and document changes and approvals in the device master record (21 CFR 820.181).

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 device-related adverse events) (21 CFR Part 803) for devices or postmarketing safety reporting (21 CFR Part 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reporting-combination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR Part 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR Parts 1000-1050.

All medical devices, including Class I and unclassified devices and combination product device constituent parts are required to be in compliance with the final Unique Device Identification System rule ("UDI Rule"). The UDI Rule requires, among other things, that a device bear a unique device identifier (UDI) on its label and package (21 CFR 801.20(a)) unless an exception or alternative applies (21 CFR 801.20(b)) and that the dates on the device label be formatted in accordance with 21 CFR 801.18. The UDI Rule (21 CFR 830.300(a) and 830.320(b)) also requires that certain information be submitted to the Global Unique Device Identification Database (GUDID) (21 CFR Part 830 Subpart E). For additional information on these requirements, please see the UDI System webpage at https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/unique-device-identification-system-udi-system.

Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-devices/medical-device-safety/medical-device-reporting-mdr-how-report-medical-device-problems.

For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-

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K253010 - Gretchen Hinchley
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assistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email ([e-mail]) or phone [phone] or 301-796-7100).

Sincerely,

Thomas Mcnamara -S

For: Christopher Ferreira, M.S.
Assistant Director
DHT6C: Division of Restorative, Repair and Trauma Devices
OHT6: Office of Orthopedic Devices
Office of Product Evaluation and Quality
Center for Devices and Radiological Health

Enclosure

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Mini Superhawk Suture Anchor System
Page 7 of 27

| Indications for Use | | |
| --- | --- | --- |
| Please type in the marketing application/submission number, if it is known. This
textbox will be left blank for original applications/submissions. | K253010 | ? |
| Please provide the device trade name(s). | | ? |
| Mini Superhawk Suture Anchor System | | |
| Please provide your Indications for Use below. | | ? |
| The Mini Superhawk Suture Anchors are intended to be used for fixation of suture (soft tissue) to bone in
the shoulder, foot/ankle, hip, knee, hand/wrist, and elbow in the following procedures: | | |
| - Shoulder: Rotator Cuff Repair, Bankart Repair, SLAP Lesion Repair, Biceps Tenodesis, Acromio-
Clavicular Separation Repair, Deltoid Repair, Capsular Shift or Capsulolabral Reconstruction. | | |
| - Foot/Ankle: Lateral Stabilization, Medial Stabilization, Achilles Tendon Repair, Hallux Valgus
Reconstruction, Mid-foot Reconstruction, Metatarsal Ligament Repair/Tendon Repair, Bunionectomy,
Digital Tendon Transfers. | | |
| - Knee: Medial Collateral Ligament Repair, Lateral Collateral Ligament Repair, Vastus Medialis Obliquus
Advancement, Patellar Tendon Repair, Posterior Oblique Ligament Repair, Iliotibial Band Tenodesis, Joint
Capsule Closure. | | |
| - Hand/Wrist: Scapholunate Ligament Reconstruction, Ulnar or Radial Collateral Ligament Reconstruction. | | |
| - Elbow: Biceps Tendon Reattachment, Tennis Elbow Repair, Ulnar or Radial Collateral Ligament
Reconstruction, Lateral Epicondylitis Repair. | | |
| - Hip: Capsular Repair, Acetabular Labral Repair. | | |
| Please select the types of uses (select one or both, as
applicable). | ☑ Prescription Use (Part 21 CFR 801 Subpart D)
☐ Over-The-Counter Use (21 CFR 801 Subpart C) | ? |

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510(k) Submission:
K253010
Page 1 of 3

# 510(k) SUMMARY

**DATE PREPARED:** September 16, 2025

**SUBMITTER INFORMATION:** Responsive Arthroscopy, Inc.
701 N. 3rd Street, Suite 208
Minneapolis, MN 55401

**ESTABLISHMENT REGISTRATION:** 3015200759

**CONTACT INFORMATION:** Gretchen Hinchley
VP of Quality, Regulatory and Compliance
[phone]
[e-mail]

**DEVICE INFORMATION:**

- **Trade Name:** Mini Superhawk Suture Anchor System
- **Common Name:** Suture Anchor
- **Classification Name:** Smooth or threaded metallic bone fixation fastener
- **Product Code:** MBI
- **Classification:** Class II
- **Regulation Number:** 21 CFR 888.3040
- **Primary Predicate Device:** Responsive Arthroscopy Knotless Push-in Suture Anchor System (K202153)
- **Additional Predicate Device:** Responsive Arthroscopy Mustang Suture Anchors (K222763)

The predicate devices have not been subject to any design-related recalls.

**DEVICE DESCRIPTION:**

The Mini Superhawk Suture Anchors are anchor devices comprised of polyether ether ketone (PEEK) material that are designed for the fixation of soft tissue to bone. The subject Mini Superhawk system features one 3.75mm diameter Screw-in (start) suture anchor preloaded on an inserter with a 1.5mm suture tape and one knotless 3.75mm diameter Push-in suture anchor preloaded on an inserter with a suture pull tab. The Push-in anchor also includes an auxiliary #0 suture that holds the anchor in place on the inserter until use and is then discarded. The Mini Superhawk Suture Anchors and inserters are assembled as a kit and provided to the end user sterile via ethylene oxide (EO) sterilization.

**INDICATIONS FOR USE:**

The Mini Superhawk Suture Anchors are intended to be used for fixation of suture (soft tissue) to bone in the shoulder, foot/ankle, hip, knee, hand/wrist, and elbow in the following procedures:

- Shoulder: Rotator Cuff Repair, Bankart Repair, SLAP Lesion Repair, Biceps Tenodesis, Acromio-Clavicular Separation Repair, Deltoid Repair, Capsular Shift or Capsulolabral Reconstruction.

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510(k) Submission:
K253010
Page 2 of 3

- Foot/Ankle: Lateral Stabilization, Medial Stabilization, Achilles Tendon Repair, Hallux Valgus Reconstruction, Mid-foot Reconstruction, Metatarsal Ligament Repair/Tendon Repair, Bunionectomy, Digital Tendon Transfers.
- Knee: Medial Collateral Ligament Repair, Lateral Collateral Ligament Repair, Vastus Medialis Obliquus Advancement, Patellar Tendon Repair, Posterior Oblique Ligament Repair, Iliotibial Band Tenodesis, Joint Capsule Closure.
- Hand/Wrist: Scapholunate Ligament Reconstruction, Ulnar or Radial Collateral Ligament Reconstruction.
- Elbow: Biceps Tendon Reattachment, Tennis Elbow Repair, Ulnar or Radial Collateral Ligament Reconstruction, Lateral Epicondylitis Repair.
- Hip: Capsular Repair, Acetabular Labral Repair.

## TECHNOLOGICAL CHARACTERISTICS:

The subject Mini Superhawk Suture Anchors have the same intended use and fundamental scientific technology as the predicate devices cleared under K202153 and K222763. The subject devices feature similar technological characteristics as the predicate devices, including PEEK anchor design, knotless suture locking, principles of operation, materials, repair suture offerings, packaging and shelf life, and sterilization method. In addition, both the subject devices and predicate devices are provided sterile and single use only pre-loaded on inserters.

The subject device features slight differences in technology as compared to the predicate devices, including anchor body geometry and dimensions, and the addition of a smaller diameter screw-in suture anchor. However, these technological characteristics are deemed equivalent to the predicate devices and have no impact on the ability of the subject devices to fulfill their intended use.

## SUBSTANTIAL EQUIVALENCE:

The subject Mini Superhawk Suture Anchors have the same intended use, indications for use, and fundamental scientific technology as the predicate devices. The minor differences in technology do not raise different questions of safety or efficacy. Therefore, the Mini Superhawk Suture Anchors are substantially equivalent to the predicate devices.

## PERFORMANCE TESTING:

Nonclinical performance testing was completed to demonstrate that the subject Mini Superhawk Suture Anchors met the established performance characteristics and design requirements. Performance testing consisted of design verification testing (bench testing) that included comparison to the predicate devices. All testing met acceptance criteria and demonstrated that the devices met design specifications and performed as intended.

The following bench testing was performed on the subject devices:

- Insertion Torque Testing (Screw-in Anchor)
- Insertion Force Testing (Push-in Anchor)
- Suture Locking Force Testing (Push-in Anchor)
- Cyclic Pullout Force Testing (both Anchors)

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K253010
510(k) Submission:
Page 3 of 3

In summary, performance testing of the Mini Superhawk Suture Anchors indicated no new risks and demonstrated substantial equivalence in performance compared to the legally marketed predicate devices.

## CONCLUSION:

In conclusion, the subject devices have the same intended use, indications for use, and fundamental scientific technology as the predicate devices. The differences in technological characteristics raise no new or different issues of safety and effectiveness, and performance testing has demonstrated that the subject devices are at least as safe and effective as the predicate devices. Therefore, the subject devices are substantially equivalent to the predicate devices.