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Seitz Solution Unlar Head

FDA UDI

Class II (US FDA UDI)

by Kapp Surgical Instrument, Inc.

Identity

Trade Name
Seitz Solution Unlar Head FDA UDI
Generic Name
Wrist ulna-head prosthesis FDA UDI
Device Name
7.5x1mm Spacer FDA UDI
Model / Reference
KCS-71 FDA UDI
Description
7.5x1mm Spacer FDA UDI

Identifiers

Catalog Number
KCS-71 FDA UDI
Primary DI / UDI-DI
B033KCS71 FDA UDI
510(k) Number
K033930 FDA UDI
FDA Product Code
KXE FDA UDI
GMDN Term
Wrist ulna-head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Wrist ulna-head prosthesis

Seitz Solution Unlar Head by Kapp Surgical Instrument, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wrist ulna-head prosthesis.

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 031042dc-9e32-4f13-a87b-7b474f14ad24 35 fields · synced Jun 9, 2026