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Arthroscope

FDA product code HRX · 670 cleared devices

Class 2 Orthopedic
Regulation
21 CFR 888.1100
Review panel
OR
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1977-04-26 – 2026-08-28

Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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