Continuum® Trilogy® Allofit® Longevity® 00-8755-011-36
by Zimmer, Inc.
Listed
Valid until
Not applicable
FDA recalls
1 ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00889024150935 | Date17 Sep 2015 | StatusListed |
Recalls
-
- Ongoing Z-2519-2023
The outer package labeling and product etch are for a Size 6, however, the implant is a Size 4, and vice versa.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Continuum® Trilogy® Allofit® Longevity®
- Generic Name
- Non-constrained polyethylene acetabular liner
- Model / Ref / Catalog
- 00-8755-011-36
- Primary DI / UDI-DI
- 00889024150935
- FDA Product Code
- LPH, JDI, LZO
- GMDN Term
- Non-constrained polyethylene acetabular liner
- Device Class
- Class II
- Regulation Number
- 888.3358, 888.3350, 888.3353
- GUDID distribution status
- In Commercial Distribution
- MRI Safety
- MR Conditional
- Size
- Lumen/Inner Diameter — 36 Millimeter
Other devices from Zimmer, Inc.
Properties
Other properties (8)
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No