Zimmer Arthroscopy System
by Zimmer, Inc.
510(k) K811596
Zimmer Arthroscopy System is a Class II device made by Zimmer, Inc., cleared under FDA 510(k) K811596 on 25 Jun 1981, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK811596 | Date25 Jun 1981 | StatusActive |
Official records
- FDA 510(k) database K811596
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- HRX
- Device class
- Class II
- Regulation
- 21 CFR Part 888.1100
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
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Other devices filed under FDA product code HRX (Arthroscope).
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