510(k) K063275
- Device
- DISTAL CLAVICULAR FRAGMENT IMMOBILIZATION PLATE LEFT, MODEL 1810-116_126-03 (05,07) RIGHT 1811-116_126-03 (05,07)
- Applicant
- Terray Corp.
- 510(k) number
- K063275
- Product code
- HRS
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2007-07-27
- Date received
- 2006-10-30
- Regulation
- 888.3030
- Classification name
- Plate, Fixation, Bone
- Medical specialty
- Orthopedic
- Review panel
- Orthopedic
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Statement
- Third party reviewed
- N
Applicant Contact#
- Contact
- STEVEN WILLIS
- Address
- 49 Jackson Ln. Pine Grove Industrial Park Arnprior CA K7S 3G8 K7S 3G8
FDA Registration Numbers#
- 1221051
- 2245304
- 3009923578
- 3010068573
- 3013843055
- 9610921
- 3009662565
- 3011127597
- 3003541440
- 3005562917
- 8010099
- 3010041511
- 3011295718
- 1020279
- 3004369035
- 3009973699
- 3010041430
- 3007420745
- 2030624
- 3009959868
- 3014315669
- 3033519208
- 1313525
- 3027339877
- 3006783837
- 3007289093
- 3014302784
- 3016237080
- 2249615
- 3004142400
- 3009812190
- 3000170817
- 3014937101
- 3022159082
- 1319429
- 1528646
- 3010726901
- 3016778139
- 2531477
- 3004549189
- 3004153896
- 2183785
- 3013756169
- 9680515
- 3007738812
- 1526439
- 3011187779
- 3014273424
- 9611281
- 3017980495
- 3010032903
- 1043653
- 1720929
- 3016247852
- 3008534770
- 3010673777
- 3012491394
- 3013014058
- 3015230955
- 3009158523
- 3005004799
- 3011580264
- 3011354099
- 3004187715
- 1828464
- 1833506
- 1835831
- 3005874553
- 3016759112
- 3007334927
- 3006946279
- 2032830
- 3007125392
- 3010123172
- 3008572101
- 3002579136
- 3019455
- 1818910
- 9614438
Source Documents#
510(k) summary PDF not indicated by FDA
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