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Jts Extendible Distal Femoral Implant

FDA UDI

Class II (US FDA UDI)

by Onkos Surgical, Inc.

Identity

Trade Name
JTS EXTENDIBLE DISTAL FEMORAL IMPLANT FDA UDI
Generic Name
Surgical mallet FDA UDI
Device Name
Hammer FDA UDI
Model / Reference
imham FDA UDI
Description
Hammer FDA UDI

Identifiers

Catalog Number
IMHAM FDA UDI
Primary DI / UDI-DI
B278IMHAM0 FDA UDI
510(k) Number
K092138 FDA UDI
K133152 FDA UDI
FDA Product Code
KRO FDA UDI
GMDN Term
Surgical mallet FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3510 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical mallet

Jts Extendible Distal Femoral Implant by Onkos Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical mallet.

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 0b16a01e-9e9b-4a63-b3be-05b3204d6b1e 35 fields · synced May 29, 2026