Identity
- Trade Name
- Symmetry Surgical FDA UDI
- Generic Name
- Soft-tissue surgical hook, reusable FDA UDI
- Device Name
- Symmetry® Hook, Lumbar, Sharp Toothed Shaft, 70 mm FDA UDI
- Model / Reference
- 59-1083S FDA UDI
- Description
- Symmetry® Hook, Lumbar, Sharp Toothed Shaft, 70 mm FDA UDI
Identifiers
- Catalog Number
- 59-1083S FDA UDI
- Primary DI / UDI-DI
- 00887482105337 FDA UDI
- 510(k) Number
- K161004 FDA UDI
- FDA Product Code
- GZT FDA UDI
- GMDN Term
- Soft-tissue surgical hook, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4800 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 70 Millimeter FDA UDI
Category: Soft-tissue surgical hook, reusable
Symmetry Surgical by Symmetry Surgical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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
- Symmetry Surgical Inc.
Sources (1)
- FDA UDI 1d90f391-23cc-4acc-a0ad-61cf263a14a9 37 fields · synced May 30, 2026