Identity
- Trade Name
- LCP FDA UDI
- Generic Name
- Orthopaedic fixation plate, non-bioabsorbable FDA UDI
- Device Name
- 4.5MM LCP® CONDYLAR PLATE 16 HOLES/350MM-LEFT FDA UDI
- Model / Reference
- 222.667 FDA UDI
- Description
- 4.5MM LCP® CONDYLAR PLATE 16 HOLES/350MM-LEFT FDA UDI
Identifiers
- Catalog Number
- 222667 FDA UDI
- Primary DI / UDI-DI
- 10886982157508 FDA UDI
- 510(k) Number
- K000066 FDA UDI
- FDA Product Code
- HTY FDA UDIHRS FDA UDIHWC FDA UDIJDW FDA UDI
- GMDN Term
- Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI888.3030 FDA UDI
- Commercial Distribution
- Not 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
Lcp by Synthes (u.s.a.) Lp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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
- Synthes (u.s.a.) Lp
Sources (1)
- FDA UDI 45a1e0b8-7a22-4af8-8efc-211bf9bb353f 37 fields · synced Jun 1, 2026