Identity
- Trade Name
- PERCUTANEOUS COMPRESSION PLATE (PC.C.P) FDA UDI
- Generic Name
- General internal orthopaedic fixation system implantation kit FDA UDI
- Device Name
- GOTFRIED PC.C.P. MAIN SLEEVE FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- GOTFRIED PC.C.P. MAIN SLEEVE FDA UDI
Identifiers
- Catalog Number
- 195000 FDA UDI
- Primary DI / UDI-DI
- 18032568865868 FDA UDI
- 510(k) Number
- K983814 FDA UDI
- FDA Product Code
- JDO FDA UDI
- GMDN Term
- General internal orthopaedic fixation system implantation kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: General internal orthopaedic fixation system implantation kit
Percutaneous Compression Plate (pc.c.p) by Orthofix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as General internal orthopaedic fixation system implantation kit.
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Cleared under the same submission
K983814 also covers:
- PERCUTANEOUS COMPRESSION PLATE (PC.C.P) — Orthofix, Inc.
- PERCUTANEOUS COMPRESSION PLATE (PC.C.P) — Orthofix, Inc.
- PERCUTANEOUS COMPRESSION PLATE (PC.C.P) — Orthofix, Inc.
- PERCUTANEOUS COMPRESSION PLATE (PC.C.P) — Orthofix, Inc.
- PERCUTANEOUS COMPRESSION PLATE (PC.C.P) — Orthofix, Inc.
- PERCUTANEOUS COMPRESSION PLATE (PC.C.P) — Orthofix, Inc.
- PERCUTANEOUS COMPRESSION PLATE (PC.C.P) — Orthofix, Inc.
- PERCUTANEOUS COMPRESSION PLATE (PC.C.P) — Orthofix, Inc.
- PERCUTANEOUS COMPRESSION PLATE (PC.C.P) — Orthofix, Inc.
- PERCUTANEOUS COMPRESSION PLATE (PC.C.P) — Orthofix, Inc.
- PERCUTANEOUS COMPRESSION PLATE (PC.C.P) — Orthofix, Inc.
- PERCUTANEOUS COMPRESSION PLATE (PC.C.P) — Orthofix, 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
- Orthofix, Inc.
Sources (1)
- FDA UDI e9332e1a-fc32-44a9-949c-6bc26bbdc398 36 fields · synced May 30, 2026