Identity
- Trade Name
- AMT Initial Placement Kit FDA UDI
- Generic Name
- Surgical depth gauge, single-use FDA UDI
- Device Name
- AMT Initial Placement Kit (12-18FR) FDA UDI
- Model / Reference
- IP-1218 FDA UDI
- Description
- AMT Initial Placement Kit (12-18FR) FDA UDI
Identifiers
- Catalog Number
- IP-1218 FDA UDI
- Primary DI / UDI-DI
- 00842071131425 FDA UDI
- 510(k) Number
- K073034 FDA UDI
- FDA Product Code
- KNT FDA UDI
- GMDN Term
- Surgical depth gauge, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5980 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
No
FDA UDI
Category: Scalpel, single-useGastro-urological guidewire, single-useEndoscopic-access dilator, single-useSurgical depth gauge, single-use
AMT Initial Placement Kit by Applied Medical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical depth gauge, single-use.
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- CrossRoads Screw System — CROSSROADS EXTREMITY SYSTEMS LLC · Class I
- General Instrument — ALPHATEC SPINE, INC. · Class I
- FuzeFix Large — FUSION ORTHOPEDICS, LLC · Class I
- Solanas — ALPHATEC SPINE, INC. · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- DVR® CROSSLOCK EPAK™DEPTH GAUGE — Biomet Orthopedics, Inc. · Class I
- FuzeFix Mini — FUSION ORTHOPEDICS, LLC · Class I
Cleared under the same submission
K073034 also covers:
- AMT Initial Placement Dilator Set — Applied Medical Technology, Inc.
- AMT Initial Placement Dilator Set — Applied Medical Technology, Inc.
- AMT Initial Placement Dilator Set — Applied Medical Technology, Inc.
- AMT Initial Placement Dilator Set — Applied Medical Technology, Inc.
- AMT Initial Placement Kit — Applied Medical Technology, Inc.
- AMT Initial Placement Kit — Applied Medical Technology, Inc.
- AMT Initial Placement Kit — Applied Medical Technology, Inc.
- AMT PEG-Assist — Applied Medical Technology, 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
- Applied Medical Technology, Inc.
Sources (1)
- FDA UDI bf7c241b-897d-4ab6-b764-750a70cd9fe5 37 fields · synced Jun 9, 2026