510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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HRRClass I

Scissors, Orthopedic, Surgical

21 CFR 888.4540 / Orthopedic
FDA source (opens on fda.gov)

HRR is the FDA product code for Scissors, Orthopedic, Surgical, a class I device type, regulated under 21 CFR 888.4540. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
HRR
Device name
Scissors, Orthopedic, Surgical
Regulation
21 CFR 888.4540
Device class
Class I
Review panel
Orthopedic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
8
Ingested recalls
1

Clearances, product code HRR

By decision year
8 clearances under product code HRR with a decision year between 1980 and 1989, 1989 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code HRR by decision year
YearClearances
19801
19841
19851
19872
19893

Applicants with the most clearances

Product code HRR
Applicants holding the most 510(k) clearances under product code HRR
ApplicantClearances
Kinetic Medical Products3
Arthropedics, Inc.2
All-Hands Medical Supply, Inc.1
Artiberia1
Edward Weck, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 176 companies shown, in name order