Identity
- Trade Name
- PolyLock Midfoot FDA UDI
- Generic Name
- Bone-resection orthopaedic reamer, single-use FDA UDI
- Device Name
- Window Joint Seeker Universal (Sterile) FDA UDI
- Model / Reference
- TN-MF-7052-S FDA UDI
- Description
- Window Joint Seeker Universal (Sterile) FDA UDI
Identifiers
- Catalog Number
- TN-MF-7052-S FDA UDI
- Primary DI / UDI-DI
- 00840124514775 FDA UDI
- 510(k) Number
- K211843 FDA UDI
- FDA Product Code
- HWC FDA UDI
- GMDN Term
- Bone-resection orthopaedic reamer, single-use 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
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
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Bone-resection orthopaedic reamer, single-use
PolyLock Midfoot by Fusion Orthopedics, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone-resection orthopaedic reamer, single-use.
- RAZOR Single-Use Acetabular Reamer — Razor Medical Instruments, Inc. · Class I
- RAZOR Single-Use Acetabular Reamer — Razor Medical Instruments, Inc. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- Disposable — Biomet Orthopedics, Inc. · Class I
- PANTA® — Newdeal Sas · Class I
- ACETABULAR REAMER EVO 2 Ti CUP D42 mm — HPF SRL · Class I
- Arthrex® — Arthrex, Inc. · Class I
- Tools - UFC — Trimed, INC. · Class I
Cleared under the same submission
K211843 also covers:
- FuzeFix Chamfered Screws — FUSION ORTHOPEDICS, LLC
- LapiLock — FUSION ORTHOPEDICS, LLC
- PolyLock — FUSION ORTHOPEDICS, LLC
- PolyLock — FUSION ORTHOPEDICS, LLC
- PolyLock — FUSION ORTHOPEDICS, LLC
- PolyLock — FUSION ORTHOPEDICS, LLC
- PolyLock — FUSION ORTHOPEDICS, LLC
- PolyLock — FUSION ORTHOPEDICS, LLC
- PolyLock — FUSION ORTHOPEDICS, LLC
- PolyLock — FUSION ORTHOPEDICS, LLC
- PolyLock — FUSION ORTHOPEDICS, LLC
- PolyLock — FUSION ORTHOPEDICS, 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
- Fusion Orthopedics, Llc
Sources (1)
- FDA UDI 209903a4-d785-41c4-a7d1-2bf98100fdee 35 fields · synced May 30, 2026