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Mustang Knotless Vented Suture Anchor

FDA UDI

Class II (US FDA UDI)

by Responsive Orthopedics Llc

Identity

Trade Name
Mustang Knotless Vented Suture Anchor FDA UDI
Generic Name
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Device Name
Mustang Knotless Vented Suture Anchor, 4.75mm FDA UDI
Model / Reference
285947 FDA UDI
Description
Mustang Knotless Vented Suture Anchor, 4.75mm FDA UDI

Identifiers

Catalog Number
285947 FDA UDI
Primary DI / UDI-DI
00811714036359 FDA UDI
510(k) Number
K222763 FDA UDI
FDA Product Code
MBI FDA UDI
GMDN Term
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Tendon/ligament bone anchor, non-bioabsorbable

Mustang Knotless Vented Suture Anchor by Responsive Orthopedics Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tendon/ligament bone anchor, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 801c76ca-60b4-452f-9c2f-5aba66d8b9ee 35 fields · synced May 30, 2026