Identity
- Trade Name
- Titan Modular Shoulder System 2.5 FDA UDI
- Generic Name
- Stem-fixed metallic humeral head prosthesis FDA UDI
- Device Name
- LOCKING BODY SCREW NON-STERLIE FDA UDI
- Model / Reference
- BSW-0920-01NS FDA UDI
- Description
- LOCKING BODY SCREW NON-STERLIE FDA UDI
Identifiers
- Catalog Number
- BSW-0920-01NS FDA UDI
- Primary DI / UDI-DI
- 00885556859520 FDA UDI
- FDA Product Code
- HSD FDA UDIKWS FDA UDI
- GMDN Term
- Stem-fixed metallic humeral head prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3690 FDA UDI888.3660 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
Moist Heat or Steam Sterilization FDA UDI
Category: Stem-fixed metallic humeral head prosthesis
Titan Modular Shoulder System 2.5 by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Stem-fixed metallic humeral head prosthesis.
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Cleared under the same submission
K142413 also covers:
- Integra® — Ascension Orthopedics, Inc.
- Titan™ — Ascension Orthopedics, Inc.
- Titan™ — Ascension Orthopedics, Inc.
- Titan™ — Ascension Orthopedics, Inc.
- Titan™ Total Shoulder System — Ascension Orthopedics, Inc.
- Titan™ Total Shoulder System — Ascension Orthopedics, Inc.
- Titan™ Total Shoulder System — Ascension Orthopedics, Inc.
- Titan™ Total Shoulder System — Ascension Orthopedics, Inc.
- Titan™ Total Shoulder System — Ascension Orthopedics, Inc.
- Titan™ Total Shoulder System — Ascension Orthopedics, Inc.
- Titan™ Total Shoulder System — Ascension Orthopedics, Inc.
- Titan™ Total Shoulder System — Ascension Orthopedics, Inc.
K213827 also covers:
- Katalyst Biopolar Radial Head System — Smith & Nephew, Inc.
- Katalyst Bipolar Radial Head System — Smith & Nephew, Inc.
- Modular Radial Head (MRH) System — Smith & Nephew, Inc.
- Modular Radial Head (MRH) System — Smith & Nephew, Inc.
- Modular Radial Head (MRH) System — Smith & Nephew, Inc.
- Titan Humeral Resurfacing Arthroplasty — Smith & Nephew, Inc.
- Titan Humeral Resurfacing Arthroplasty — Smith & Nephew, Inc.
- Titan Modular Shoulder System — Smith & Nephew, Inc.
- Titan Modular Shoulder System — Smith & Nephew, Inc.
- Titan Modular Shoulder System 2.5 — Smith & Nephew, Inc.
- Titan Modular Shoulder System 2.5 — Smith & Nephew, Inc.
- Titan Modular Shoulder System 2.5 — Smith & Nephew, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI 7aedc724-f7b2-4107-a0cc-9e99c9c9a035 37 fields · synced Jun 8, 2026