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Hornet Biostinger

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
HORNET BIOSTINGER FDA UDI
Generic Name
Meniscus screw FDA UDI
Device Name
13MM HORNET DISPOSABLE INSERTER, BIOSTINGER IMPLANT FDA UDI
Model / Reference
C8360 FDA UDI
Description
13MM HORNET DISPOSABLE INSERTER, BIOSTINGER IMPLANT FDA UDI

Identifiers

Catalog Number
C8360 FDA UDI
Primary DI / UDI-DI
20845854013486 FDA UDI
510(k) Number
K020377 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Meniscus screw 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

No

FDA UDI

Dimensions & Sizes

Size
Length — 13 Millimeter FDA UDI

Category: Meniscus screw

Hornet Biostinger by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Meniscus screw.

Cleared under the same submission

K020377 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 83a9db27-7bb3-43c6-aeaf-6b5d772f078d 37 fields · synced Jun 8, 2026