Identity
- Trade Name
- Augmented BP Rmr Gd Inserter FDA UDI
- Generic Name
- Surgical instrument handle, non-torque-limiting FDA UDI
- Model / Reference
- SSI005400 FDA UDI
Identifiers
- Catalog Number
- SSI005400 FDA UDI
- Primary DI / UDI-DI
- 00889024583047 FDA UDI
- 510(k) Number
- K060694 FDA UDI
- FDA Product Code
- KWT FDA UDIKWS FDA UDI
- GMDN Term
- Surgical instrument handle, non-torque-limiting FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3650 FDA UDI888.3660 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
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical instrument handle, non-torque-limiting
Augmented BP Rmr Gd Inserter by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Surgical instrument handle, non-torque-limiting.
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Cleared under the same submission
K060694 also covers:
- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
- COMPREHENSIVE SHOULDER SYSTEM — Biomet Orthopedics, 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
- Biomet Orthopedics, Inc.
Sources (1)
- FDA UDI 528a7ce1-5dbf-40d8-8e0a-0d2f725ea70b 35 fields · synced May 30, 2026