Identity
- Trade Name
- Hammerdesis™ Interphalangeal Fusion System FDA UDI
- Generic Name
- Orthopaedic bone pin, non-bioabsorbable FDA UDI
- Device Name
- 1.1mm K-Wire FDA UDI
- Model / Reference
- HMR-116-01 FDA UDI
- Description
- 1.1mm K-Wire FDA UDI
Identifiers
- Primary DI / UDI-DI
- G079HMR116010 FDA UDI
- 510(k) Number
- K231147 FDA UDI
- FDA Product Code
- HTY FDA UDI
- GMDN Term
- Orthopaedic bone pin, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Commercial Distribution
- 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
Category: Orthopaedic bone pin, non-bioabsorbable
Hammerdesis™ Interphalangeal Fusion System by Intelivation, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic bone pin, non-bioabsorbable.
- Steinmann Pins, K-Wire, smooth — Gebr. Brasseler GmbH & Co. KG · Class II
- KW03-310-18.A — newbox medical GmbH · Class IIb
- Steinmann Pins, K-Wire, smooth — Gebr. Brasseler GmbH & Co. KG · Class II
- IlluminOss — ILLUMINOSS MEDICAL INC. · Class II
- XtraFix® External Fixation System — Zimmer, Inc. · Class II
- CALIBRATED GUIDE WIRE, THREADED TROCAR POINT — Biomet Orthopedics, Inc. · Class II
- TRAUMA FIXATION SYSTEMS — Biomet Orthopedics, Inc. · Class II
- SMART TSF — Smith & Nephew, Inc. · Class II
Cleared under the same submission
K231147 also covers:
- Hammerdesis™ Interphalangeal Fusion System — Intelivation, LLC
- Hammerdesis™ Interphalangeal Fusion System — Intelivation, LLC
- Hammerdesis™ Interphalangeal Fusion System — Intelivation, LLC
- Hammerdesis™ Interphalangeal Fusion System — Intelivation, LLC
- Hammerdesis™ Interphalangeal Fusion System — Intelivation, LLC
- Hammerdesis™ Interphalangeal Fusion System — Intelivation, LLC
- Hammerdesis™ Interphalangeal Fusion System — Intelivation, LLC
- Hammerdesis™ Interphalangeal Fusion System — Intelivation, LLC
- Hammerdesis™ Interphalangeal Fusion System — Intelivation, LLC
- Hammerdesis™ Interphalangeal Fusion System — Intelivation, LLC
- Hammerdesis™ Interphalangeal Fusion System — Intelivation, LLC
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
- Intelivation, LLC
Sources (1)
- FDA UDI 0a352426-2e35-474b-9e78-9fe6d09efc6c 34 fields · synced Jun 8, 2026