Identity
- Trade Name
- TM Slot Guide FDA UDI
- Generic Name
- Bone-coring punch, reusable FDA UDI
- Model / Reference
- SSI005885 FDA UDI
Identifiers
- Catalog Number
- SSI005885 FDA UDI
- Primary DI / UDI-DI
- 00889024588929 FDA UDI
- 510(k) Number
- K172767 FDA UDI
- FDA Product Code
- KWS FDA UDIKWT FDA UDI
- GMDN Term
- Bone-coring punch, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3660 FDA UDI888.3650 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Bone-coring punch, reusable
TM Slot Guide by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K172767 also covers:
- TM Cruciate Punch — Zimmer, Inc.
- TM Cruciate Punch — Zimmer, Inc.
- TM Cruciate Punch — Zimmer, Inc.
- TM Handle — Zimmer, Inc.
- TM Punch — Zimmer, Inc.
- TM Punch — Zimmer, Inc.
- TM Slot Guide — Zimmer, Inc.
- TM Slot Guide — Zimmer, Inc.
- TMR+ Bowtie Baseplate Reamer — Zimmer, Inc.
- Threaded Steinmann Pin — Zimmer, Inc.
- Trabecular Metal Reverse Plus™ — Zimmer, Inc.
- Trabecular Metal Reverse Plus™ — Zimmer, 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
- Zimmer, Inc.
Sources (1)
- FDA UDI 45add7e9-8ae9-4450-8513-996c126a0abd 36 fields · synced Jun 8, 2026