21 CFR 874.3540
§ 874.3540 Prosthesis modification instrument for ossicular replacement surgery.
United States · 21 CFR — Food and Drugs · Status: effective
Cite this
- Citation
- 21 CFR 874.3540, § 874.3540 Prosthesis modification instrument for ossicular replacement surgery, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/90222
- Permanent ID
ys:prov:90222@1- SHA-256
75fb79f271e3d96f5c55efca6afc4a553ac650f987722d04942c80a82824b8ff
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Full text
(a) Identification. A prosthesis modification instrument for ossicular replacement surgery is a device intended for use by a surgeon to construct ossicular replacements. This generic type of device includes the ear, nose, and throat cutting block; wire crimper, wire bending die; wire closure forceps; piston cutting jib; gelfoam TM punch; wire cutting scissors; and ossicular finger vise.
(b) Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to § 874.9. If the device is not labeled or otherwise represented as sterile, it is exempt from the current good manufacturing practice requirements of the quality management system regulation in part 820 of this chapter, except for requirements concerning records and complaint files under § 820.35 of this chapter.
Legislative history
This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.