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Coated Revision Stem

FDA UDI

Class II (US FDA UDI)

by Signal Medical Corp.

Identity

Trade Name
Coated Revision Stem FDA UDI
Generic Name
Sleeve femoral/tibial extension, coated FDA UDI
Device Name
10x150 Coated Revision Stem FDA UDI
Model / Reference
10x150 FDA UDI
Description
10x150 Coated Revision Stem FDA UDI

Identifiers

Catalog Number
22-08-1110150 FDA UDI
Primary DI / UDI-DI
B046220811101500 FDA UDI
510(k) Number
K100370 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Sleeve femoral/tibial extension, coated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Sleeve femoral/tibial extension, coated

Coated Revision Stem by Signal Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sleeve femoral/tibial extension, coated.

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 e782e0b5-19c8-4317-9146-cb26bbdf178b 36 fields · synced May 31, 2026