Identity
- Trade Name
- PerFuse™ Percutaneous Decompression System FDA UDI
- Generic Name
- Orthopaedic trocar blade, single-use FDA UDI
- Model / Reference
- 800-0541 FDA UDI
Identifiers
- Catalog Number
- 800-0541 FDA UDI
- Primary DI / UDI-DI
- 00887868263026 FDA UDI
- 510(k) Number
- K141762 FDA UDI
- FDA Product Code
- FMF FDA UDI
- GMDN Term
- Orthopaedic trocar blade, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5860 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Orthopaedic trocar blade, single-use
PerFuse™ Percutaneous Decompression System by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic trocar blade, single-use.
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- OTHER EXTERNAL FIXATION — Smith & Nephew, Inc. · Class II
- Decima Spine Instrument Kit — DECIMA SPINE, INC. · Class I
- Orthopaedic Surgical Instruments — Citieffe · Class I
- DISTRACTION, INTERNAL, STERILE — KLS-Martin L.P. · Class I
Cleared under the same submission
K141762 also covers:
- PERFUSE — Biomet Biologics, LLC
- PERFUSE — Biomet Biologics, LLC
- PERFUSE — Biomet Biologics, LLC
- PERFUSE DECOMPRESSION INSTRUMENTATION — Biomet Biologics, LLC
- PERFUSE HANDLE ASSEMBLY — Biomet Biologics, LLC
- PERFUSE STRIKE CAP — Biomet Biologics, LLC
- Perfuse™ Decompression System — Biomet Biologics, LLC
- PerFuse™ Decompression System — Biomet Orthopedics, Inc.
- PerFuse™ Decompression System — Biomet Orthopedics, Inc.
- PerFuse™ Decompression System — Biomet Orthopedics, Inc.
- PerFuse™ Decompression System — Biomet Orthopedics, Inc.
- Perfuse — 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 2f930cc1-b9ff-408e-87de-29ee1027a7ba 35 fields · synced May 30, 2026