510(k) K771744
- Device
- OSTEOTOMES FOR CUTTING BONH
- Applicant
- Depuy, Inc.
- 510(k) number
- K771744
- Product code
- HWM
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-09-28
- Date received
- 1977-09-15
- Regulation
- 878.4800
- Classification name
- Osteotome
- Medical specialty
- General, Plastic Surgery
- Review panel
- General, Plastic Surgery
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 4221 Richmond Rd., NW Walker MI US 49534 49534
FDA Registration Numbers#
- 1219518
- 8040278
- 3003694247
- 3002976036
- 8010372
- 3009189869
- 3009380063
- 1824199
- 1649390
- 3010041511
- 3010370500
- 3016438694
- 3012447612
- 9680515
- 3006563559
- 3014763043
- 1720747
- 1450662
- 3015882686
- 3011600579
- 8040179
- 3008114965
- 3006801265
- 3004215117
- 8030607
- 8010300
- 3023657851
- 8010528
- 3013011598
- 3024988980
- 1835998
- 9680837
- 3015451162
- 3005751028
- 1056350
- 1649379
- 3004608878
- 1032347
- 3038195984
- 9611616
- 3007648354
- 9611274
- 9681622
- 3015212339
- 3008812560
- 2953359
- 3012234585
- 3011015572
- 3005440795
- 1222188
- 3003431869
- 3013875765
- 3011137372
- 3008711893
- 8039053
- 1030489
- 1526439
- 8010379
- 3005809810
- 1057425
- 3010009693
- 1424478
- 3006554912
- 1935627
- 3002808270
- 3010235355
- 3012130008
- 1000426080
- 8010591
- 3038503932
- 9680059
- 8010155
- 3005061536
- 3009959868
- 1834331
- 1221934
- 3009513193
- 8010303
- 9611461
- 8044098
Source Documents#
510(k) summary PDF not indicated by FDA