Identity
- Trade Name
- MiniHip Stem FDA UDI
- Generic Name
- Bone curette, reusable FDA UDI
- Device Name
- Curette FDA UDI
- Model / Reference
- 580.9500 FDA UDI
- Description
- Curette FDA UDI
Identifiers
- Catalog Number
- 580.9501 FDA UDI
- Primary DI / UDI-DI
- 05055196949676 FDA UDI
- 510(k) Number
- K083312 FDA UDI
- FDA Product Code
- LZO FDA UDI
- GMDN Term
- Bone curette, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3353 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
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: Bone curette, reusable
MiniHip Stem by Corin Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Bone curette, reusable.
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- Novo Surgical — NOVO SURGICAL, INC. · Class I
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- Volkmann Bone Curette Oval - Fig. 00 17 cm - 6 3/4" Scoop Size 4.4 mm Stainless Steel — SURTEX INSTRUMENTS LTD · Class I
Cleared under the same submission
K083312 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Corin Ltd
Sources (1)
- FDA UDI 361089aa-3ed3-4636-b42b-63b24bd9835a 36 fields · synced Jun 1, 2026