Identity
- Trade Name
- OsseoFit™ Subscapularis Kit (Bone Tunnel) FDA UDI
- Generic Name
- Polyolefin/fluoropolymer suture, monofilament FDA UDI
- Device Name
- Subscapularis Repair Suture Kit-Bone Tunnel FDA UDI
- Model / Reference
- 120002051 FDA UDI
- Description
- Subscapularis Repair Suture Kit-Bone Tunnel FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840277405005 FDA UDI
- GMDN Term
- Polyolefin/fluoropolymer suture, monofilament FDA UDI
Classification
- 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
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Polyolefin/fluoropolymer suture, monofilamentPolyolefin/fluoropolymer suture, multifilament
OsseoFit™ Subscapularis Kit (Bone Tunnel) by Riverpoint Medical Llc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Riverpoint Medical Llc
Sources (1)
- FDA UDI d4f27782-264e-4de3-be28-0d3d64a5f6c4 33 fields · synced May 30, 2026