510(k) K202659
- Device
- Stryker Arthroscope
- Applicant
- Stryker
- 510(k) number
- K202659
- Product code
- HRX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2020-12-01
- Date received
- 2020-09-14
- Regulation
- 888.1100
- Classification name
- Arthroscope
- Medical specialty
- Orthopedic
- Review panel
- Orthopedic
- Device class
- 2
- Clearance type
- Special
- Statement or summary
- Summary
- Third party reviewed
- No
Related Records
Applicant Contact
- Contact
- Christie Samsa
- Address
- 5900 Optical Ct. San Jose CA US 95138 95138
FDA Registration Numbers
- 3005820796
- 1221485
- 9617601
- 1526611
- 3006946348
- 3015316279
- 3011373951
- 3013404959
- 8040700
- 1423395
- 3013700547
- 3007113251
- 3010400367
- 3008110533
- 2020601
- 3025318945
- 2936485
- 2032521
- 1421101
- 9681191
- 1054241
- 3008868758
- 2245304
- 1928237
- 3014725904
- 3010097171
- 3016667340
- 1032347
- 3010120148
- 3009538961
- 9611665
- 3008959444
- 1220477
- 3009888740
- 3008583793
- 9614434
- 3010273872
- 3011163668
- 3018242561
- 3009417901
- 9617616
- 2085947
- 2032677
- 2084346
- 3011230048
- 3006142527
- 1528668
- 1422078
- 1061124
- 3015967359
- 3009704301
- 3030733800
- 2320762
- 3004215117
- 3020746799
- 2916714
- 3002807310
- 1834331
- 3002808022
- 1030489
- 3005528784
- 1424263
- 3011024991
- 9614841
- 2434839
- 3015219237
- 3012818475
- 3011543740
- 3013176080
- 3014202166
- 3035366890
- 9681477
- 3014388471
- 2032098
- 3006524618
- 3016099036
- 3004464325
- 2650143
- 3006561161
Source Documents
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